ENST00000261937.11:c.3986G>A
MANE Select
|
ENSP00000261937.6:p.Gly1329Asp
|
|
ENST00000261937.10:c.3986G>A
|
ENSP00000261937.6:p.Gly1329Asp
|
|
ENST00000502603.5:n.686G>A
|
|
|
NM_182925.4:c.3986G>A
|
NP_891555.2:p.Gly1329Asp
|
|
XM_011534477.1:c.4235G>A
|
XP_011532779.1:p.Gly1412Asp
|
|
XM_011534478.1:c.4217G>A
|
XP_011532780.1:p.Gly1406Asp
|
|
XM_011534482.1:c.4004G>A
|
XP_011532784.1:p.Gly1335Asp
|
|
XM_011534483.1:c.3926G>A
|
XP_011532785.1:p.Gly1309Asp
|
|
XM_011534484.1:c.3527G>A
|
XP_011532786.1:p.Gly1176Asp
|
|
XR_941095.1:n.4272G>A
|
|
|
XM_011534478.3:c.4217G>A
|
XP_011532780.1:p.Gly1406Asp
|
|
XM_011534484.2:c.3527G>A
|
XP_011532786.1:p.Gly1176Asp
|
|
XM_017009263.1:c.*132G>A
|
XP_016864752.1:n.*132G>A
|
|
XM_017009268.1:c.3908G>A
|
XP_016864757.1:p.Gly1303Asp
|
|
XR_001742050.2:n.4476G>A
|
|
|
NM_182925.5:c.3986G>A
MANE Select
|
NP_891555.2:p.Gly1329Asp
|
|