|
NM_152342.4:c.1210G>T
MANE Select
|
NP_689555.2:p.Val404Phe
|
|
ENST00000570137.7:c.1210G>T
MANE Select
|
ENSP00000476295.1:p.Val404Phe
|
|
NM_152342.2:c.1210G>T
|
NP_689555.2:p.Val404Phe
|
|
NM_152342.3:c.1210G>T
|
NP_689555.2:p.Val404Phe
|
|
ENST00000562812.5:c.1213G>T
|
ENSP00000454546.1:p.Val405Phe
|
|
ENST00000563890.5:c.1213G>T
|
ENSP00000455111.1:p.Val405Phe
|
|
ENST00000566173.3:c.1213G>T
|
ENSP00000456934.1:p.Val405Phe
|
|
ENST00000570137.6:c.1210G>T
|
ENSP00000476295.1:p.Val404Phe
|
|
XM_011522866.1:c.1312G>T
|
XP_011521168.1:p.Val438Phe
|
|
XM_011522867.1:c.1201G>T
|
XP_011521169.1:p.Val401Phe
|
|
XM_011522867.2:c.1201G>T
|
XP_011521169.1:p.Val401Phe
|
|
XM_011522868.1:c.1033G>T
|
XP_011521170.1:p.Val345Phe
|
|
XM_024450151.1:c.1033G>T
|
XP_024305919.1:p.Val345Phe
|