ENST00000306010.8:c.676G>A
|
ENSP00000302111.7:p.Ala226Thr
|
|
ENST00000651593.1:c.583G>A
MANE Select
|
ENSP00000498729.1:p.Ala195Thr
|
|
ENST00000306010.7:c.676G>A
|
ENSP00000302111.7:p.Ala226Thr
|
|
NM_002412.3:c.676G>A
|
NP_002403.2:p.Ala226Thr
|
|
NM_002412.4:c.676G>A
|
NP_002403.2:p.Ala226Thr
|
|
XM_005252682.2:c.583G>A
|
XP_005252739.1:p.Ala195Thr
|
|
XM_006717863.2:c.406G>A
|
XP_006717926.1:p.Ala136Thr
|
|
XM_011539817.1:c.592G>A
|
XP_011538119.1:p.Ala198Thr
|
|
NM_002412.5:c.583G>A
MANE Select
|
NP_002403.3:p.Ala195Thr
|
|
XM_017016275.1:c.406G>A
|
XP_016871764.1:p.Ala136Thr
|
|