ENST00000409959.8:c.4623G=
MANE Select
|
ENSP00000386787.3:p.Pro1541=
|
|
ENST00000240487.5:c.3954G=
|
ENSP00000240487.5:p.Pro1318=
|
|
ENST00000409663.7:c.4620G=
|
ENSP00000386574.3:p.Pro1540=
|
|
ENST00000409959.7:c.4623G=
|
ENSP00000386787.3:p.Pro1541=
|
|
NM_001131007.1:c.4623G=
|
NP_001124479.1:p.Pro1541=
|
|
NM_015196.3:c.4620G=
|
NP_056011.3:p.Pro1540=
|
|
XM_005262871.3:c.2745G=
|
XP_005262928.2:p.Pro915=
|
|
XM_011531780.1:c.4710G=
|
XP_011530082.1:p.Pro1570=
|
|
XM_011531781.1:c.4707G=
|
XP_011530083.1:p.Pro1569=
|
|
XM_011531782.1:c.4680G=
|
XP_011530084.1:p.Pro1560=
|
|
XM_011531783.1:c.4458G=
|
XP_011530085.1:p.Pro1486=
|
|
XM_017007925.1:c.4620G=
|
XP_016863414.1:p.Pro1540=
|
|
XM_017007926.1:c.4617G=
|
XP_016863415.1:p.Pro1539=
|
|
XM_024453956.1:c.4680G=
|
XP_024309724.1:p.Pro1560=
|
|
XM_024453957.1:c.4677G=
|
XP_024309725.1:p.Pro1559=
|
|
XM_024453958.1:c.2745G=
|
XP_024309726.1:p.Pro915=
|
|
NM_001131007.2:c.4623G=
MANE Select
|
NP_001124479.1:p.Pro1541=
|
|
NM_015196.4:c.4620G=
|
NP_056011.3:p.Pro1540=
|
|