ENST00000278612.9:c.37+2493T>G
MANE Select
|
ENSP00000278612.8:n.37+2493T>G
|
|
ENST00000278612.8:c.37+2493T>G
|
ENSP00000278612.8:n.37+2493T>G
|
|
ENST00000531384.1:c.37+2493T>G
|
ENSP00000433497.1:n.37+2493T>G
|
|
ENST00000610253.5:n.137+2493T>G
|
|
|
NM_002519.2:c.37+2493T>G
|
NP_002510.2:n.37+2493T>G
|
|
XM_011542854.1:c.37+2493T>G
|
XP_011541156.1:n.37+2493T>G
|
|
XM_011542855.1:c.37+2493T>G
|
XP_011541157.1:n.37+2493T>G
|
|
NM_001321307.1:c.37+2493T>G
|
NP_001308236.1:n.37+2493T>G
|
|
XM_011542854.2:c.37+2493T>G
|
XP_011541156.1:n.37+2493T>G
|
|
NM_002519.3:c.37+2493T>G
MANE Select
|
NP_002510.2:n.37+2493T>G
|
|