ENST00000525346.6:c.1133T>G
|
ENSP00000435707.3:p.Ile378Ser
|
|
ENST00000526780.6:c.1133T>G
|
ENSP00000435668.2:p.Ile378Ser
|
|
ENST00000527316.6:c.959T>G
|
ENSP00000435047.2:p.Ile320Ser
|
|
ENST00000682708.1:c.1184T>G
|
ENSP00000506866.1:p.Ile395Ser
|
|
ENST00000683287.1:c.1169T>G
|
ENSP00000507607.1:p.Ile390Ser
|
|
ENST00000683714.1:c.1141T>G
|
ENSP00000508207.1:p.Ser381Ala
|
|
ENST00000684396.1:n.1173T>G
|
|
|
ENST00000685320.1:c.548T>G
|
ENSP00000509319.1:p.Ile183Ser
|
|
ENST00000690257.1:c.1037T>G
|
ENSP00000510750.1:p.Ile346Ser
|
|
ENST00000355527.8:c.1133T>G
MANE Select
|
ENSP00000347717.4:p.Ile378Ser
|
|
ENST00000355527.7:c.1133T>G
|
ENSP00000347717.3:p.Ile378Ser
|
|
ENST00000407721.6:c.1133T>G
|
ENSP00000384739.2:p.Ile378Ser
|
|
ENST00000525137.1:c.634T>G
|
ENSP00000435956.1:p.Ser212Ala
|
|
ENST00000533800.5:c.383T>G
|
ENSP00000435011.1:p.Ile128Ser
|
|
ENST00000534795.5:c.319+2142T>G
|
|
|
NM_001163817.1:c.1133T>G
|
NP_001157289.1:p.Ile378Ser
|
|
NM_001360.2:c.1133T>G , LRG_340t1:c.1133T>G
|
NP_001351.2:p.Ile378Ser
|
|
XM_011544777.1:c.1267T>G
|
XP_011543079.1:p.Ser423Ala
|
|
XM_011544777.2:c.1267T>G
|
XP_011543079.1:p.Ser423Ala
|
|
NM_001163817.2:c.1133T>G
|
NP_001157289.1:p.Ile378Ser
|
|
NM_001360.3:c.1133T>G
MANE Select
|
NP_001351.2:p.Ile378Ser
|
|