ENST00000703783.1:n.884A>G
|
|
|
ENST00000703785.1:n.965A>G
|
|
|
ENST00000262464.9:c.4100A>G
MANE Select
|
ENSP00000262464.4:p.Asp1367Gly
|
|
ENST00000262464.8:c.4100A>G
|
ENSP00000262464.4:p.Asp1367Gly
|
|
ENST00000507835.5:c.650A>G
|
ENSP00000426839.1:p.Asp217Gly
|
|
ENST00000508053.5:c.4100A>G
|
ENSP00000424571.1:p.Asp1367Gly
|
|
ENST00000508989.5:c.4001A>G
|
ENSP00000425596.1:p.Asp1334Gly
|
|
ENST00000619499.4:c.4097A>G
|
ENSP00000482132.1:p.Asp1366Gly
|
|
NM_001999.3:c.4100A>G
|
NP_001990.2:p.Asp1367Gly
|
|
XM_017009228.2:c.3947A>G
|
XP_016864717.1:p.Asp1316Gly
|
|
NM_001999.4:c.4100A>G
MANE Select
|
NP_001990.2:p.Asp1367Gly
|
|