ENST00000375687.10:c.3987_3988insA
MANE Select
|
ENSP00000364839.4:p.Pro1330ThrfsTer?
|
|
ENST00000646985.1:c.3804_3805insA
|
ENSP00000495053.1:p.Pro1269ThrfsTer?
|
|
ENST00000647223.1:n.6340_6341insA
|
|
|
ENST00000651418.1:c.1870-1731_1870-1730insA
|
ENSP00000499150.1:n.1870-1731_1870-1730insA
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|
ENST00000306058.9:c.3972_3973insA
|
ENSP00000305119.5:p.Pro1325ThrfsTer?
|
|
ENST00000375687.8:c.3987_3988insA
|
ENSP00000364839.4:p.Pro1330ThrfsTer?
|
|
ENST00000613218.4:c.3987_3988insA
|
ENSP00000480487.1:p.Pro1330ThrfsTer?
|
|
ENST00000620121.4:c.3987_3988insA
|
ENSP00000481978.1:p.Pro1330ThrfsTer?
|
|
NM_015338.5:c.3987_3988insA , LRG_630t1:c.3987_3988insA
|
NP_056153.2:p.Pro1330ThrfsTer?
|
|
XM_006723727.2:c.3984_3985insA
|
XP_006723790.1:p.Pro1329ThrfsTer?
|
|
XM_006723728.2:c.3957_3958insA
|
XP_006723791.1:p.Pro1320ThrfsTer?
|
|
XM_006723730.2:c.3903_3904insA
|
XP_006723793.1:p.Pro1302ThrfsTer?
|
|
XM_006723732.2:c.3804_3805insA
|
XP_006723795.1:p.Pro1269ThrfsTer?
|
|
XM_006723733.1:c.3303_3304insA
|
XP_006723796.1:p.Pro1102ThrfsTer?
|
|
XM_011528647.1:c.4251_4252insA
|
XP_011526949.1:p.Pro1418ThrfsTer?
|
|
XM_011528648.1:c.4248_4249insA
|
XP_011526950.1:p.Pro1417ThrfsTer?
|
|
XM_011528649.1:c.4167_4168insA
|
XP_011526951.1:p.Pro1390ThrfsTer?
|
|
XM_011528650.1:c.4098_4099insA
|
XP_011526952.1:p.Pro1367ThrfsTer?
|
|
XM_011528651.1:c.3966_3967insA
|
XP_011526953.1:p.Pro1323ThrfsTer?
|
|
XM_011528652.1:c.3903_3904insA
|
XP_011526954.1:p.Pro1302ThrfsTer?
|
|
NM_001363734.1:c.3804_3805insA
|
NP_001350663.1:p.Pro1269ThrfsTer?
|
|
XM_006723727.3:c.3984_3985insA
|
XP_006723790.1:p.Pro1329ThrfsTer?
|
|
XM_006723728.3:c.3957_3958insA
|
XP_006723791.1:p.Pro1320ThrfsTer?
|
|
XM_006723730.4:c.3903_3904insA
|
XP_006723793.1:p.Pro1302ThrfsTer?
|
|
XM_011528648.3:c.4248_4249insA
|
XP_011526950.1:p.Pro1417ThrfsTer?
|
|
XM_011528652.2:c.3903_3904insA
|
XP_011526954.1:p.Pro1302ThrfsTer?
|
|
XM_017027704.1:c.3903_3904insA
|
XP_016883193.1:p.Pro1302ThrfsTer?
|
|
XM_017027705.1:c.3903_3904insA
|
XP_016883194.1:p.Pro1302ThrfsTer?
|
|
XM_017027706.1:c.3834_3835insA
|
XP_016883195.1:p.Pro1279ThrfsTer?
|
|
NM_015338.6:c.3987_3988insA
MANE Select
|
NP_056153.2:p.Pro1330ThrfsTer?
|
|