ENST00000394975.3:c.*93G>T
MANE Select
|
ENSP00000378426.2:n.*93G>T
|
|
ENST00000300851.10:c.*196G>T
|
ENSP00000300851.6:n.*196G>T
|
|
ENST00000319788.11:c.*196G>T
|
ENSP00000326135.7:n.*196G>T
|
|
ENST00000354895.4:c.*196G>T
|
ENSP00000346969.4:n.*196G>T
|
|
ENST00000394975.2:c.*93G>T
|
ENSP00000378426.2:n.*93G>T
|
|
ENST00000420057.2:c.547G>T
|
|
|
ENST00000529564.1:c.283+2271G>T
|
ENSP00000431371.1:n.283+2271G>T
|
|
ENST00000532364.1:c.173+3516G>T
|
ENSP00000460316.1:n.173+3516G>T
|
|
ENST00000533518.5:c.407+51G>T
|
|
|
NM_001311311.1:c.*93G>T
|
NP_001298240.1:n.*93G>T
|
|
NM_024006.4:c.*93G>T
|
NP_076869.1:n.*93G>T
|
|
NM_024006.5:c.*93G>T
|
NP_076869.1:n.*93G>T
|
|
NM_206824.1:c.*196G>T
|
NP_996560.1:n.*196G>T
|
|
NM_206824.2:c.*196G>T
|
NP_996560.1:n.*196G>T
|
|
XM_011545944.1:c.*93G>T
|
XP_011544246.1:n.*93G>T
|
|
XM_011545945.1:c.*196G>T
|
XP_011544247.1:n.*196G>T
|
|
XR_950848.1:n.1373G>T
|
|
|
NM_024006.6:c.*93G>T
MANE Select
|
NP_076869.1:n.*93G>T
|
|
NM_001311311.2:c.*93G>T
|
NP_001298240.1:n.*93G>T
|
|
NM_206824.3:c.*196G>T
|
NP_996560.1:n.*196G>T
|
|