ENST00000703783.1:n.916T>G
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|
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ENST00000703785.1:n.997T>G
|
|
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ENST00000262464.9:c.4132T>G
MANE Select
|
ENSP00000262464.4:p.Cys1378Gly
|
|
ENST00000262464.8:c.4132T>G
|
ENSP00000262464.4:p.Cys1378Gly
|
|
ENST00000507835.5:c.682T>G
|
ENSP00000426839.1:p.Cys228Gly
|
|
ENST00000508053.5:c.4132T>G
|
ENSP00000424571.1:p.Cys1378Gly
|
|
ENST00000508989.5:c.4033T>G
|
ENSP00000425596.1:p.Cys1345Gly
|
|
ENST00000619499.4:c.4129T>G
|
ENSP00000482132.1:p.Cys1377Gly
|
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NM_001999.3:c.4132T>G
|
NP_001990.2:p.Cys1378Gly
|
|
XM_017009228.2:c.3979T>G
|
XP_016864717.1:p.Cys1327Gly
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|
NM_001999.4:c.4132T>G
MANE Select
|
NP_001990.2:p.Cys1378Gly
|
|