ENST00000432791.7:c.532G>A
MANE Select
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ENSP00000387393.3:p.Gly178Arg
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ENST00000571698.2:c.532G>A
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ENSP00000459330.2:p.Gly178Arg
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ENST00000572904.6:c.532G>A
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ENSP00000461484.1:p.Gly178Arg
|
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ENST00000574590.6:c.532G>A
|
ENSP00000461812.2:p.Gly178Arg
|
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ENST00000574655.6:n.786G>A
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ENST00000575318.6:c.532G>A
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ENSP00000461299.1:p.Gly178Arg
|
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ENST00000638269.1:n.776G>A
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ENST00000638275.1:c.532G>A
|
ENSP00000492576.1:p.Gly178Arg
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ENST00000638902.1:n.636G>A
|
|
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ENST00000639099.1:n.782G>A
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|
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ENST00000639150.1:c.23+52059G>A
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ENSP00000491906.1:n.23+52059G>A
|
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ENST00000639356.1:n.782G>A
|
|
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ENST00000639375.1:n.770G>A
|
|
|
ENST00000639531.1:c.532G>A
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ENSP00000491765.1:p.Gly178Arg
|
|
ENST00000648792.1:c.532G>A
|
ENSP00000497628.1:p.Gly178Arg
|
|
ENST00000262419.10:c.532G>A
|
ENSP00000262419.6:p.Gly178Arg
|
|
ENST00000432791.5:c.532G>A
|
ENSP00000387393.2:p.Gly178Arg
|
|
ENST00000572904.5:c.532G>A
|
ENSP00000461484.1:p.Gly178Arg
|
|
ENST00000574590.5:c.532G>A
|
ENSP00000461812.1:p.Gly178Arg
|
|
ENST00000575318.5:c.532G>A
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ENSP00000461299.1:p.Gly178Arg
|
|
NM_001193465.1:c.532G>A
|
NP_001180394.1:p.Gly178Arg
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|
NM_001193466.1:c.532G>A
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NP_001180395.1:p.Gly178Arg
|
|
NM_015443.3:c.532G>A
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NP_056258.1:p.Gly178Arg
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XM_006721823.1:c.532G>A
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XP_006721886.1:p.Gly178Arg
|
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XM_006721824.2:c.532G>A
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XP_006721887.1:p.Gly178Arg
|
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XM_011524628.1:c.532G>A
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XP_011522930.1:p.Gly178Arg
|
|
XM_011524629.1:c.532G>A
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XP_011522931.1:p.Gly178Arg
|
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XM_011524630.1:c.532G>A
|
XP_011522932.1:p.Gly178Arg
|
|
XM_011524631.1:c.532G>A
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XP_011522933.1:p.Gly178Arg
|
|
XM_006721823.2:c.532G>A
|
XP_006721886.1:p.Gly178Arg
|
|
XM_006721824.4:c.532G>A
|
XP_006721887.1:p.Gly178Arg
|
|
XM_011524628.3:c.532G>A
|
XP_011522930.1:p.Gly178Arg
|
|
XM_011524629.3:c.532G>A
|
XP_011522931.1:p.Gly178Arg
|
|
XM_011524630.3:c.532G>A
|
XP_011522932.1:p.Gly178Arg
|
|
XM_011524631.3:c.532G>A
|
XP_011522933.1:p.Gly178Arg
|
|
XM_017024488.2:c.532G>A
|
XP_016879977.1:p.Gly178Arg
|
|
XM_017024489.1:c.532G>A
|
XP_016879978.1:p.Gly178Arg
|
|
NM_001193466.2:c.532G>A
|
NP_001180395.1:p.Gly178Arg
|
|
NM_015443.4:c.532G>A
MANE Select
|
NP_056258.1:p.Gly178Arg
|
|
NM_001193465.2:c.532G>A
|
NP_001180394.1:p.Gly178Arg
|
|
NM_001379198.1:c.532G>A
|
NP_001366127.1:p.Gly178Arg
|
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