ENST00000703783.1:n.380T>G
|
|
|
ENST00000703785.1:n.461T>G
|
|
|
ENST00000262464.9:c.3596T>G
MANE Select
|
ENSP00000262464.4:p.Val1199Gly
|
|
ENST00000262464.8:c.3596T>G
|
ENSP00000262464.4:p.Val1199Gly
|
|
ENST00000507835.5:c.146T>G
|
ENSP00000426839.1:p.Val49Gly
|
|
ENST00000508053.5:c.3596T>G
|
ENSP00000424571.1:p.Val1199Gly
|
|
ENST00000508989.5:c.3497T>G
|
ENSP00000425596.1:p.Val1166Gly
|
|
ENST00000619499.4:c.3593T>G
|
ENSP00000482132.1:p.Val1198Gly
|
|
NM_001999.3:c.3596T>G
|
NP_001990.2:p.Val1199Gly
|
|
XM_017009228.2:c.3443T>G
|
XP_016864717.1:p.Val1148Gly
|
|
NM_001999.4:c.3596T>G
MANE Select
|
NP_001990.2:p.Val1199Gly
|
|