ENST00000432791.7:c.2520A>T
MANE Select
|
ENSP00000387393.3:p.Ser840=
|
|
ENST00000572904.6:c.2520A>T
|
ENSP00000461484.1:p.Ser840=
|
|
ENST00000573286.2:n.4203A>T
|
|
|
ENST00000574590.6:c.2520A>T
|
ENSP00000461812.2:p.Ser840=
|
|
ENST00000575318.6:c.2331A>T
|
ENSP00000461299.1:p.Ser777=
|
|
ENST00000576137.2:n.517A>T
|
|
|
ENST00000638275.1:c.2331A>T
|
ENSP00000492576.1:p.Ser777=
|
|
ENST00000639150.1:c.1254A>T
|
ENSP00000491906.1:p.Ser418=
|
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ENST00000639467.1:c.183A>T
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ENSP00000492741.1:p.Ser61=
|
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ENST00000639531.1:c.2331A>T
|
ENSP00000491765.1:p.Ser777=
|
|
ENST00000640636.1:c.473A>T
|
|
|
ENST00000648792.1:c.2520A>T
|
ENSP00000497628.1:p.Ser840=
|
|
ENST00000262419.10:c.2520A>T
|
ENSP00000262419.6:p.Ser840=
|
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ENST00000432791.5:c.2520A>T
|
ENSP00000387393.2:p.Ser840=
|
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ENST00000572218.5:n.6737A>T
|
|
|
ENST00000572904.5:c.2520A>T
|
ENSP00000461484.1:p.Ser840=
|
|
ENST00000573286.1:n.376A>T
|
|
|
ENST00000574590.5:c.2520A>T
|
ENSP00000461812.1:p.Ser840=
|
|
ENST00000575318.5:c.2331A>T
|
ENSP00000461299.1:p.Ser777=
|
|
ENST00000576137.1:n.159A>T
|
|
|
ENST00000576870.5:n.492A>T
|
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NM_001193465.1:c.2520A>T
|
NP_001180394.1:p.Ser840=
|
|
NM_001193466.1:c.2520A>T
|
NP_001180395.1:p.Ser840=
|
|
NM_015443.3:c.2520A>T
|
NP_056258.1:p.Ser840=
|
|
XM_006721823.1:c.2520A>T
|
XP_006721886.1:p.Ser840=
|
|
XM_006721824.2:c.2520A>T
|
XP_006721887.1:p.Ser840=
|
|
XM_011524628.1:c.2520A>T
|
XP_011522930.1:p.Ser840=
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XM_011524629.1:c.2418A>T
|
XP_011522931.1:p.Ser806=
|
|
XM_011524630.1:c.2331A>T
|
XP_011522932.1:p.Ser777=
|
|
XM_011524631.1:c.2331A>T
|
XP_011522933.1:p.Ser777=
|
|
XM_011524632.1:c.1290A>T
|
XP_011522934.1:p.Ser430=
|
|
XM_006721823.2:c.2520A>T
|
XP_006721886.1:p.Ser840=
|
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XM_006721824.4:c.2520A>T
|
XP_006721887.1:p.Ser840=
|
|
XM_011524628.3:c.2520A>T
|
XP_011522930.1:p.Ser840=
|
|
XM_011524629.3:c.2418A>T
|
XP_011522931.1:p.Ser806=
|
|
XM_011524630.3:c.2331A>T
|
XP_011522932.1:p.Ser777=
|
|
XM_011524631.3:c.2331A>T
|
XP_011522933.1:p.Ser777=
|
|
XM_011524632.3:c.1290A>T
|
XP_011522934.1:p.Ser430=
|
|
XM_017024488.2:c.2331A>T
|
XP_016879977.1:p.Ser777=
|
|
XM_017024489.1:c.2418A>T
|
XP_016879978.1:p.Ser806=
|
|
NM_001193466.2:c.2520A>T
|
NP_001180395.1:p.Ser840=
|
|
NM_015443.4:c.2520A>T
MANE Select
|
NP_056258.1:p.Ser840=
|
|
NM_001193465.2:c.2520A>T
|
NP_001180394.1:p.Ser840=
|
|
NM_001379198.1:c.2520A>T
|
NP_001366127.1:p.Ser840=
|
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