ENST00000261937.11:c.4028C>A
MANE Select
|
ENSP00000261937.6:p.Pro1343Gln
|
|
ENST00000261937.10:c.4028C>A
|
ENSP00000261937.6:p.Pro1343Gln
|
|
ENST00000502603.5:n.728C>A
|
|
|
NM_182925.4:c.4028C>A
|
NP_891555.2:p.Pro1343Gln
|
|
XM_011534477.1:c.4277C>A
|
XP_011532779.1:p.Pro1426Gln
|
|
XM_011534478.1:c.4259C>A
|
XP_011532780.1:p.Pro1420Gln
|
|
XM_011534482.1:c.4046C>A
|
XP_011532784.1:p.Pro1349Gln
|
|
XM_011534483.1:c.3968C>A
|
XP_011532785.1:p.Pro1323Gln
|
|
XM_011534484.1:c.3569C>A
|
XP_011532786.1:p.Pro1190Gln
|
|
XR_941095.1:n.4314C>A
|
|
|
XM_011534478.3:c.4259C>A
|
XP_011532780.1:p.Pro1420Gln
|
|
XM_011534484.2:c.3569C>A
|
XP_011532786.1:p.Pro1190Gln
|
|
XM_017009263.1:c.*174C>A
|
XP_016864752.1:n.*174C>A
|
|
XM_017009268.1:c.3950C>A
|
XP_016864757.1:p.Pro1317Gln
|
|
XR_001742050.2:n.4518C>A
|
|
|
NM_182925.5:c.4028C>A
MANE Select
|
NP_891555.2:p.Pro1343Gln
|
|