ENST00000272371.7:c.4173T>G
MANE Select
|
ENSP00000272371.2:p.Ser1391=
|
|
ENST00000339598.8:c.1872T>G
MANE Plus Clinical
|
ENSP00000344521.3:p.Ser624=
|
|
ENST00000402415.8:c.1932T>G
|
ENSP00000383906.4:p.Ser644=
|
|
ENST00000272371.6:c.4173T>G
|
ENSP00000272371.2:p.Ser1391=
|
|
ENST00000338581.10:c.1872T>G
|
ENSP00000345137.6:p.Ser624=
|
|
ENST00000339598.7:c.1872T>G
|
ENSP00000344521.3:p.Ser624=
|
|
ENST00000402415.7:c.2103T>G
|
ENSP00000383906.3:p.Ser701=
|
|
ENST00000403946.7:c.4173T>G
|
ENSP00000385255.3:p.Ser1391=
|
|
NM_001287489.1:c.4173T>G
|
NP_001274418.1:p.Ser1391=
|
|
NM_004802.3:c.1872T>G
|
NP_004793.2:p.Ser624=
|
|
NM_194248.2:c.4173T>G
|
NP_919224.1:p.Ser1391=
|
|
NM_194322.2:c.2103T>G
|
NP_919303.1:p.Ser701=
|
|
NM_194323.2:c.1872T>G
|
NP_919304.1:p.Ser624=
|
|
XM_005264644.2:c.4158T>G
|
XP_005264701.1:p.Ser1386=
|
|
XM_011533185.1:c.4218T>G
|
XP_011531487.1:p.Ser1406=
|
|
XM_017005338.1:c.4113T>G
|
XP_016860827.1:p.Ser1371=
|
|
NM_001287489.2:c.4173T>G
|
NP_001274418.1:p.Ser1391=
|
|
NM_004802.4:c.1872T>G
|
NP_004793.2:p.Ser624=
|
|
NM_194248.3:c.4173T>G
MANE Select
|
NP_919224.1:p.Ser1391=
|
|
NM_194322.3:c.2103T>G
|
NP_919303.1:p.Ser701=
|
|
NM_194323.3:c.1872T>G
MANE Plus Clinical
|
NP_919304.1:p.Ser624=
|
|