ENST00000703783.1:n.1006+138C>G
|
|
|
ENST00000703785.1:n.1087+138C>G
|
|
|
ENST00000262464.9:c.4222+138C>G
MANE Select
|
ENSP00000262464.4:n.4222+138C>G
|
|
ENST00000262464.8:c.4222+138C>G
|
ENSP00000262464.4:n.4222+138C>G
|
|
ENST00000507835.5:c.772+138C>G
|
ENSP00000426839.1:n.772+138C>G
|
|
ENST00000508053.5:c.4222+138C>G
|
ENSP00000424571.1:n.4222+138C>G
|
|
ENST00000508989.5:c.4123+138C>G
|
ENSP00000425596.1:n.4123+138C>G
|
|
ENST00000619499.4:c.4219+138C>G
|
ENSP00000482132.1:n.4219+138C>G
|
|
NM_001999.3:c.4222+138C>G
|
NP_001990.2:n.4222+138C>G
|
|
XM_017009228.2:c.4069+138C>G
|
XP_016864717.1:n.4069+138C>G
|
|
NM_001999.4:c.4222+138C>G
MANE Select
|
NP_001990.2:n.4222+138C>G
|
|