ENST00000496887.7:c.894+9C>T
|
ENSP00000434560.2:n.894+9C>T
|
|
ENST00000646564.2:c.711+9C>T
|
ENSP00000495806.2:n.711+9C>T
|
|
ENST00000155840.12:c.1251+9C>T
MANE Select
|
ENSP00000155840.2:n.1251+9C>T
|
|
ENST00000335475.6:c.870+9C>T
|
ENSP00000334497.5:n.870+9C>T
|
|
ENST00000646564.1:c.357+9C>T
|
ENSP00000495806.1:n.357+9C>T
|
|
ENST00000155840.9:c.1251+9C>T
|
ENSP00000155840.2:n.1251+9C>T
|
|
ENST00000335475.5:c.870+9C>T
|
ENSP00000334497.5:n.870+9C>T
|
|
NM_000218.2:c.1251+9C>T , LRG_287t1:c.1251+9C>T
|
NP_000209.2:n.1251+9C>T
|
|
NM_181798.1:c.870+9C>T , LRG_287t2:c.870+9C>T
|
NP_861463.1:n.870+9C>T
|
|
NM_000218.3:c.1251+9C>T
MANE Select
|
NP_000209.2:n.1251+9C>T
|
|