|
NM_181486.4:c.1084C>T
MANE Select
|
NP_852259.1:p.Gln362Ter
|
|
ENST00000405440.7:c.1084C>T
MANE Select
|
ENSP00000384152.3:p.Gln362Ter
|
|
NM_000192.3:c.1084C>T , LRG_670t1:c.1084C>T
|
NP_000183.2:p.Gln362Ter
|
|
NM_080717.2:c.934C>T
|
NP_542448.1:p.Gln312Ter
|
|
NM_080717.3:c.934C>T
|
NP_542448.1:p.Gln312Ter
|
|
NM_080717.4:c.934C>T
|
NP_542448.1:p.Gln312Ter
|
|
NM_181486.2:c.1084C>T
|
NP_852259.1:p.Gln362Ter
|
|
ENST00000310346.8:c.1084C>T
|
ENSP00000309913.4:p.Gln362Ter
|
|
ENST00000349716.9:c.934C>T
|
ENSP00000337723.5:p.Gln312Ter
|
|
ENST00000405440.6:c.1084C>T
|
ENSP00000384152.2:p.Gln362Ter
|
|
XM_017019912.1:c.1132C>T
|
XP_016875401.1:p.Gln378Ter
|