ENST00000697124.1:n.896G>C
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ENST00000219596.6:c.1775G>C
MANE Select
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ENSP00000219596.1:p.Gly592Ala
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ENST00000219596.5:c.1775G>C
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ENSP00000219596.1:p.Gly592Ala
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|
ENST00000339854.8:c.1235G>C
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ENSP00000339639.4:p.Gly412Ala
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ENST00000536379.5:c.1142G>C
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ENSP00000445079.1:p.Gly381Ala
|
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ENST00000536980.5:c.*51G>C
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ENSP00000444178.1:n.*51G>C
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ENST00000537682.5:c.*51G>C
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ENSP00000438611.1:n.*51G>C
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ENST00000538326.5:c.*400G>C
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ENSP00000437486.1:n.*400G>C
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ENST00000539145.5:c.696G>C
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ENSP00000444471.1:n.696G>C
|
|
ENST00000541159.5:c.1317G>C
|
ENSP00000438711.1:p.Trp439Cys
|
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ENST00000542898.5:c.*51G>C
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ENSP00000444615.1:n.*51G>C
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|
ENST00000570511.5:c.1180G>C
|
ENSP00000458312.1:n.1180G>C
|
|
ENST00000572244.5:c.465G>C
|
ENSP00000461186.1:n.465G>C
|
|
ENST00000574583.5:c.547G>C
|
ENSP00000460269.1:n.547G>C
|
|
ENST00000576315.5:c.580G>C
|
ENSP00000460551.1:n.580G>C
|
|
ENST00000621655.1:c.1312G>C
|
ENSP00000481436.1:n.1312G>C
|
|
NM_000243.2:c.1775G>C , LRG_190t1:c.1775G>C
|
NP_000234.1:p.Gly592Ala
|
|
NM_001198536.1:c.1317G>C
|
NP_001185465.1:p.Trp439Cys
|
|
XM_017023236.2:c.1772G>C
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XP_016878725.1:p.Gly591Ala
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XR_001751903.1:n.2082G>C
|
|
|
NM_000243.3:c.1775G>C
MANE Select
|
NP_000234.1:p.Gly592Ala
|
|
NM_001198536.2:c.1317G>C
|
NP_001185465.2:p.Trp439Cys
|
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