ENST00000375687.10:c.3921T>C
MANE Select
|
ENSP00000364839.4:p.Ser1307=
|
|
ENST00000646985.1:c.3738T>C
|
ENSP00000495053.1:p.Ser1246=
|
|
ENST00000647223.1:n.6274T>C
|
|
|
ENST00000651418.1:c.1870-1797T>C
|
ENSP00000499150.1:n.1870-1797T>C
|
|
ENST00000306058.9:c.3906T>C
|
ENSP00000305119.5:p.Ser1302=
|
|
ENST00000375687.8:c.3921T>C
|
ENSP00000364839.4:p.Ser1307=
|
|
ENST00000613218.4:c.3921T>C
|
ENSP00000480487.1:p.Ser1307=
|
|
ENST00000620121.4:c.3921T>C
|
ENSP00000481978.1:p.Ser1307=
|
|
NM_015338.5:c.3921T>C , LRG_630t1:c.3921T>C
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NP_056153.2:p.Ser1307=
|
|
XM_006723727.2:c.3918T>C
|
XP_006723790.1:p.Ser1306=
|
|
XM_006723728.2:c.3891T>C
|
XP_006723791.1:p.Ser1297=
|
|
XM_006723730.2:c.3837T>C
|
XP_006723793.1:p.Ser1279=
|
|
XM_006723732.2:c.3738T>C
|
XP_006723795.1:p.Ser1246=
|
|
XM_006723733.1:c.3237T>C
|
XP_006723796.1:p.Ser1079=
|
|
XM_011528647.1:c.4185T>C
|
XP_011526949.1:p.Ser1395=
|
|
XM_011528648.1:c.4182T>C
|
XP_011526950.1:p.Ser1394=
|
|
XM_011528649.1:c.4101T>C
|
XP_011526951.1:p.Ser1367=
|
|
XM_011528650.1:c.4032T>C
|
XP_011526952.1:p.Ser1344=
|
|
XM_011528651.1:c.3900T>C
|
XP_011526953.1:p.Ser1300=
|
|
XM_011528652.1:c.3837T>C
|
XP_011526954.1:p.Ser1279=
|
|
NM_001363734.1:c.3738T>C
|
NP_001350663.1:p.Ser1246=
|
|
XM_006723727.3:c.3918T>C
|
XP_006723790.1:p.Ser1306=
|
|
XM_006723728.3:c.3891T>C
|
XP_006723791.1:p.Ser1297=
|
|
XM_006723730.4:c.3837T>C
|
XP_006723793.1:p.Ser1279=
|
|
XM_011528648.3:c.4182T>C
|
XP_011526950.1:p.Ser1394=
|
|
XM_011528652.2:c.3837T>C
|
XP_011526954.1:p.Ser1279=
|
|
XM_017027704.1:c.3837T>C
|
XP_016883193.1:p.Ser1279=
|
|
XM_017027705.1:c.3837T>C
|
XP_016883194.1:p.Ser1279=
|
|
XM_017027706.1:c.3768T>C
|
XP_016883195.1:p.Ser1256=
|
|
NM_015338.6:c.3921T>C
MANE Select
|
NP_056153.2:p.Ser1307=
|
|