ENST00000525346.6:c.*721T>G
|
ENSP00000435707.3:n.*721T>G
|
|
ENST00000526780.6:c.*721T>G
|
ENSP00000435668.2:n.*721T>G
|
|
ENST00000682708.1:c.*721T>G
|
ENSP00000506866.1:n.*721T>G
|
|
ENST00000683287.1:c.*721T>G
|
ENSP00000507607.1:n.*721T>G
|
|
ENST00000683714.1:c.*912T>G
|
ENSP00000508207.1:n.*912T>G
|
|
ENST00000684396.1:n.2189T>G
|
|
|
ENST00000685320.1:c.*721T>G
|
ENSP00000509319.1:n.*721T>G
|
|
ENST00000690257.1:c.*721T>G
|
ENSP00000510750.1:n.*721T>G
|
|
ENST00000355527.8:c.*721T>G
MANE Select
|
ENSP00000347717.4:n.*721T>G
|
|
ENST00000355527.7:c.*721T>G
|
ENSP00000347717.3:n.*721T>G
|
|
ENST00000407721.6:c.*721T>G
|
ENSP00000384739.2:n.*721T>G
|
|
ENST00000534795.5:c.319+3158T>G
|
|
|
NM_001163817.1:c.*721T>G
|
NP_001157289.1:n.*721T>G
|
|
NM_001360.2:c.*721T>G , LRG_340t1:c.*721T>G
|
NP_001351.2:n.*721T>G
|
|
XM_011544777.1:c.*912T>G
|
XP_011543079.1:n.*912T>G
|
|
XM_011544777.2:c.*912T>G
|
XP_011543079.1:n.*912T>G
|
|
NM_001163817.2:c.*721T>G
|
NP_001157289.1:n.*721T>G
|
|
NM_001360.3:c.*721T>G
MANE Select
|
NP_001351.2:n.*721T>G
|
|