|
ENST00000375687.10:c.3883A>G
MANE Select
|
ENSP00000364839.4:p.Ser1295Gly
|
|
|
ENST00000646985.1:c.3700A>G
|
ENSP00000495053.1:p.Ser1234Gly
|
|
|
ENST00000647223.1:n.6236A>G
|
|
|
|
ENST00000651418.1:c.1870-1835A>G
|
ENSP00000499150.1:n.1870-1835A>G
|
|
|
ENST00000306058.9:c.3868A>G
|
ENSP00000305119.5:p.Ser1290Gly
|
|
|
ENST00000375687.8:c.3883A>G
|
ENSP00000364839.4:p.Ser1295Gly
|
|
|
ENST00000613218.4:c.3883A>G
|
ENSP00000480487.1:p.Ser1295Gly
|
|
|
ENST00000620121.4:c.3883A>G
|
ENSP00000481978.1:p.Ser1295Gly
|
|
|
NM_015338.5:c.3883A>G , LRG_630t1:c.3883A>G
|
NP_056153.2:p.Ser1295Gly
|
|
|
XM_006723727.2:c.3880A>G
|
XP_006723790.1:p.Ser1294Gly
|
|
|
XM_006723728.2:c.3853A>G
|
XP_006723791.1:p.Ser1285Gly
|
|
|
XM_006723730.2:c.3799A>G
|
XP_006723793.1:p.Ser1267Gly
|
|
|
XM_006723732.2:c.3700A>G
|
XP_006723795.1:p.Ser1234Gly
|
|
|
XM_006723733.1:c.3199A>G
|
XP_006723796.1:p.Ser1067Gly
|
|
|
XM_011528647.1:c.4147A>G
|
XP_011526949.1:p.Ser1383Gly
|
|
|
XM_011528648.1:c.4144A>G
|
XP_011526950.1:p.Ser1382Gly
|
|
|
XM_011528649.1:c.4063A>G
|
XP_011526951.1:p.Ser1355Gly
|
|
|
XM_011528650.1:c.3994A>G
|
XP_011526952.1:p.Ser1332Gly
|
|
|
XM_011528651.1:c.3862A>G
|
XP_011526953.1:p.Ser1288Gly
|
|
|
XM_011528652.1:c.3799A>G
|
XP_011526954.1:p.Ser1267Gly
|
|
|
NM_001363734.1:c.3700A>G
|
NP_001350663.1:p.Ser1234Gly
|
|
|
XM_006723727.3:c.3880A>G
|
XP_006723790.1:p.Ser1294Gly
|
|
|
XM_006723728.3:c.3853A>G
|
XP_006723791.1:p.Ser1285Gly
|
|
|
XM_006723730.4:c.3799A>G
|
XP_006723793.1:p.Ser1267Gly
|
|
|
XM_011528648.3:c.4144A>G
|
XP_011526950.1:p.Ser1382Gly
|
|
|
XM_011528652.2:c.3799A>G
|
XP_011526954.1:p.Ser1267Gly
|
|
|
XM_017027704.1:c.3799A>G
|
XP_016883193.1:p.Ser1267Gly
|
|
|
XM_017027705.1:c.3799A>G
|
XP_016883194.1:p.Ser1267Gly
|
|
|
XM_017027706.1:c.3730A>G
|
XP_016883195.1:p.Ser1244Gly
|
|
|
NM_015338.6:c.3883A>G
MANE Select
|
NP_056153.2:p.Ser1295Gly
|
|
