ENST00000281928.9:c.1245G=
MANE Select
|
ENSP00000281928.3:p.Val415=
|
|
ENST00000548743.2:c.1215G=
|
ENSP00000448553.2:p.Val405=
|
|
ENST00000549786.2:c.673G=
|
|
|
ENST00000647567.1:c.1152G=
|
ENSP00000497136.1:p.Val384=
|
|
ENST00000648737.1:n.1009G=
|
|
|
ENST00000650226.1:c.1245G=
|
ENSP00000496981.1:p.Val415=
|
|
ENST00000281928.7:c.1245G=
|
ENSP00000281928.3:p.Val415=
|
|
NM_015335.4:c.1245G=
|
NP_056150.1:p.Val415=
|
|
XM_011538080.1:c.1245G=
|
XP_011536382.1:p.Val415=
|
|
XM_011538081.1:c.1245G=
|
XP_011536383.1:p.Val415=
|
|
XM_011538082.1:c.1215G=
|
XP_011536384.1:p.Val405=
|
|
XM_011538080.2:c.1245G=
|
XP_011536382.1:p.Val415=
|
|
XM_011538081.2:c.1245G=
|
XP_011536383.1:p.Val415=
|
|
XM_011538082.2:c.1215G=
|
XP_011536384.1:p.Val405=
|
|
XM_017019090.1:c.1245G=
|
XP_016874579.1:p.Val415=
|
|
NM_015335.5:c.1245G=
MANE Select
|
NP_056150.1:p.Val415=
|
|