ENST00000267845.8:c.1671_1672delinsAA
MANE Select
|
ENSP00000267845.3:p.Pro558Thr
|
|
ENST00000267845.7:c.1671_1672delinsAA
|
ENSP00000267845.3:p.Pro558Thr
|
|
ENST00000543581.5:c.1572_1573delinsAA
|
ENSP00000440252.1:p.Pro525Thr
|
|
ENST00000559816.1:n.1415_1416delinsAA
|
|
|
NM_001306146.1:c.1572_1573delinsAA
|
NP_001293075.1:p.Pro525Thr
|
|
NM_002112.3:c.1671_1672delinsAA
|
NP_002103.2:p.Pro558Thr
|
|
XM_011521479.1:c.1434_1435delinsAA
|
XP_011519781.1:p.Pro479Thr
|
|
XM_011521480.1:c.1239_1240delinsAA
|
XP_011519782.1:p.Pro414Thr
|
|
XM_017022094.1:c.1776_1777delinsAA
|
XP_016877583.1:p.Pro593Thr
|
|
XM_017022095.1:c.1677_1678delinsAA
|
XP_016877584.1:p.Pro560Thr
|
|
XM_017022096.1:c.1548_1549delinsAA
|
XP_016877585.1:p.Pro517Thr
|
|
XM_017022097.1:c.1539_1540delinsAA
|
XP_016877586.1:p.Pro514Thr
|
|
XM_017022098.1:c.1344_1345delinsAA
|
XP_016877587.1:p.Pro449Thr
|
|
NM_002112.4:c.1671_1672delinsAA
MANE Select
|
NP_002103.2:p.Pro558Thr
|
|
NM_001306146.2:c.1572_1573delinsAA
|
NP_001293075.1:p.Pro525Thr
|
|