ENST00000324071.10:c.1275T>G
MANE Select
|
ENSP00000324648.2:p.Ala425=
|
|
ENST00000598834.2:c.1177-177T>G
|
|
|
ENST00000324071.8:c.1275T>G
|
ENSP00000324648.2:p.Ala425=
|
|
ENST00000593831.1:c.567T>G
|
ENSP00000470582.1:p.Ala189=
|
|
ENST00000597612.1:n.647+311T>G
|
|
|
NM_000767.4:c.1275T>G
|
NP_000758.1:p.Ala425=
|
|
XM_005258569.3:c.1152+311T>G
|
XP_005258626.1:n.1152+311T>G
|
|
XM_006723050.2:c.1275T>G
|
XP_006723113.1:p.Ala425=
|
|
XM_011526546.1:c.1153-20T>G
|
XP_011524848.1:n.1153-20T>G
|
|
XM_011526547.1:c.1153-177T>G
|
XP_011524849.1:n.1153-177T>G
|
|
XM_011526548.1:c.795T>G
|
XP_011524850.1:p.Ala265=
|
|
XM_011526549.1:c.684T>G
|
XP_011524851.1:p.Ala228=
|
|
XM_011526550.1:c.675T>G
|
XP_011524852.1:p.Ala225=
|
|
NM_000767.5:c.1275T>G
MANE Select
|
NP_000758.1:p.Ala425=
|
|