ENST00000261937.11:c.4027C>G
MANE Select
|
ENSP00000261937.6:p.Pro1343Ala
|
|
ENST00000261937.10:c.4027C>G
|
ENSP00000261937.6:p.Pro1343Ala
|
|
ENST00000502603.5:n.727C>G
|
|
|
NM_182925.4:c.4027C>G
|
NP_891555.2:p.Pro1343Ala
|
|
XM_011534477.1:c.4276C>G
|
XP_011532779.1:p.Pro1426Ala
|
|
XM_011534478.1:c.4258C>G
|
XP_011532780.1:p.Pro1420Ala
|
|
XM_011534482.1:c.4045C>G
|
XP_011532784.1:p.Pro1349Ala
|
|
XM_011534483.1:c.3967C>G
|
XP_011532785.1:p.Pro1323Ala
|
|
XM_011534484.1:c.3568C>G
|
XP_011532786.1:p.Pro1190Ala
|
|
XR_941095.1:n.4313C>G
|
|
|
XM_011534478.3:c.4258C>G
|
XP_011532780.1:p.Pro1420Ala
|
|
XM_011534484.2:c.3568C>G
|
XP_011532786.1:p.Pro1190Ala
|
|
XM_017009263.1:c.*173C>G
|
XP_016864752.1:n.*173C>G
|
|
XM_017009268.1:c.3949C>G
|
XP_016864757.1:p.Pro1317Ala
|
|
XR_001742050.2:n.4517C>G
|
|
|
NM_182925.5:c.4027C>G
MANE Select
|
NP_891555.2:p.Pro1343Ala
|
|