|
NM_021942.6:c.1381G>T
MANE Select
|
NP_068761.4:p.Glu461Ter
|
|
ENST00000334690.11:c.1381G>T
MANE Select
|
ENSP00000335371.6:p.Glu461Ter
|
|
NM_021942.5:c.1381G>T
|
NP_068761.4:p.Glu461Ter
|
|
NM_199053.2:c.1381G>T
|
NP_951008.1:p.Glu461Ter
|
|
NM_199053.3:c.1381G>T
|
NP_951008.1:p.Glu461Ter
|
|
ENST00000334690.10:c.1381G>T
|
ENSP00000335371.6:p.Glu461Ter
|
|
ENST00000357207.8:c.1381G>T
|
ENSP00000349738.4:p.Glu461Ter
|
|
ENST00000505676.5:c.348+313G>T
|
ENSP00000422915.1:n.348+313G>T
|
|
ENST00000512476.1:c.199G>T
|
ENSP00000421004.1:p.Glu67Ter
|
|
XM_011532180.1:c.1381G>T
|
XP_011530482.1:p.Glu461Ter
|
|
XM_017008537.2:c.1381G>T
|
XP_016864026.1:p.Glu461Ter
|
|
XM_017008538.2:c.1381G>T
|
XP_016864027.1:p.Glu461Ter
|
|
XM_024454179.1:c.1381G>T
|
XP_024309947.1:p.Glu461Ter
|
|
XM_024454180.1:c.1381G>T
|
XP_024309948.1:p.Glu461Ter
|
|
XM_024454181.1:c.31G>T
|
XP_024309949.1:p.Glu11Ter
|
|
XR_001741315.2:n.1573G>T
|
|