ENST00000703783.1:n.268T>G
|
|
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ENST00000703785.1:n.349T>G
|
|
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ENST00000262464.9:c.3484T>G
MANE Select
|
ENSP00000262464.4:p.Cys1162Gly
|
|
ENST00000262464.8:c.3484T>G
|
ENSP00000262464.4:p.Cys1162Gly
|
|
ENST00000507835.5:c.34T>G
|
ENSP00000426839.1:p.Cys12Gly
|
|
ENST00000508053.5:c.3484T>G
|
ENSP00000424571.1:p.Cys1162Gly
|
|
ENST00000508989.5:c.3385T>G
|
ENSP00000425596.1:p.Cys1129Gly
|
|
ENST00000619499.4:c.3481T>G
|
ENSP00000482132.1:p.Cys1161Gly
|
|
NM_001999.3:c.3484T>G
|
NP_001990.2:p.Cys1162Gly
|
|
XM_017009228.2:c.3331T>G
|
XP_016864717.1:p.Cys1111Gly
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|
NM_001999.4:c.3484T>G
MANE Select
|
NP_001990.2:p.Cys1162Gly
|
|