|
NM_015114.3:c.706C>T
MANE Select
|
NP_055929.1:p.Arg236Ter
|
|
ENST00000357997.10:c.706C>T
MANE Select
|
ENSP00000350686.5:p.Arg236Ter
|
|
NM_015114.2:c.706C>T
|
NP_055929.1:p.Arg236Ter
|
|
ENST00000357997.9:c.706C>T
|
ENSP00000350686.5:p.Arg236Ter
|
|
ENST00000539605.5:n.7205C>T
|
|
|
ENST00000545623.5:n.551C>T
|
|
|
XM_005266159.2:c.520C>T
|
XP_005266216.1:p.Arg174Ter
|
|
XM_005266159.3:c.520C>T
|
XP_005266216.1:p.Arg174Ter
|
|
XM_005266160.1:c.520C>T
|
XP_005266217.1:p.Arg174Ter
|
|
XM_005266160.2:c.520C>T
|
XP_005266217.1:p.Arg174Ter
|
|
XM_005266161.1:c.706C>T
|
XP_005266218.1:p.Arg236Ter
|
|
XM_006719735.1:c.706C>T
|
XP_006719798.1:p.Arg236Ter
|
|
XM_011534787.1:c.706C>T
|
XP_011533089.1:p.Arg236Ter
|
|
XM_011534787.3:c.706C>T
|
XP_011533089.1:p.Arg236Ter
|
|
XM_011534788.1:c.706C>T
|
XP_011533090.1:p.Arg236Ter
|
|
XM_024448899.1:c.-689C>T
|
XP_024304667.1:n.-689C>T
|
|
XR_001748638.1:n.707C>T
|
|