|
ENST00000375687.10:c.3958G>T
MANE Select
|
ENSP00000364839.4:p.Ala1320Ser
|
|
|
ENST00000646985.1:c.3775G>T
|
ENSP00000495053.1:p.Ala1259Ser
|
|
|
ENST00000647223.1:n.6311G>T
|
|
|
|
ENST00000651418.1:c.1870-1760G>T
|
ENSP00000499150.1:n.1870-1760G>T
|
|
|
ENST00000306058.9:c.3943G>T
|
ENSP00000305119.5:p.Ala1315Ser
|
|
|
ENST00000375687.8:c.3958G>T
|
ENSP00000364839.4:p.Ala1320Ser
|
|
|
ENST00000613218.4:c.3958G>T
|
ENSP00000480487.1:p.Ala1320Ser
|
|
|
ENST00000620121.4:c.3958G>T
|
ENSP00000481978.1:p.Ala1320Ser
|
|
|
NM_015338.5:c.3958G>T , LRG_630t1:c.3958G>T
|
NP_056153.2:p.Ala1320Ser
|
|
|
XM_006723727.2:c.3955G>T
|
XP_006723790.1:p.Ala1319Ser
|
|
|
XM_006723728.2:c.3928G>T
|
XP_006723791.1:p.Ala1310Ser
|
|
|
XM_006723730.2:c.3874G>T
|
XP_006723793.1:p.Ala1292Ser
|
|
|
XM_006723732.2:c.3775G>T
|
XP_006723795.1:p.Ala1259Ser
|
|
|
XM_006723733.1:c.3274G>T
|
XP_006723796.1:p.Ala1092Ser
|
|
|
XM_011528647.1:c.4222G>T
|
XP_011526949.1:p.Ala1408Ser
|
|
|
XM_011528648.1:c.4219G>T
|
XP_011526950.1:p.Ala1407Ser
|
|
|
XM_011528649.1:c.4138G>T
|
XP_011526951.1:p.Ala1380Ser
|
|
|
XM_011528650.1:c.4069G>T
|
XP_011526952.1:p.Ala1357Ser
|
|
|
XM_011528651.1:c.3937G>T
|
XP_011526953.1:p.Ala1313Ser
|
|
|
XM_011528652.1:c.3874G>T
|
XP_011526954.1:p.Ala1292Ser
|
|
|
NM_001363734.1:c.3775G>T
|
NP_001350663.1:p.Ala1259Ser
|
|
|
XM_006723727.3:c.3955G>T
|
XP_006723790.1:p.Ala1319Ser
|
|
|
XM_006723728.3:c.3928G>T
|
XP_006723791.1:p.Ala1310Ser
|
|
|
XM_006723730.4:c.3874G>T
|
XP_006723793.1:p.Ala1292Ser
|
|
|
XM_011528648.3:c.4219G>T
|
XP_011526950.1:p.Ala1407Ser
|
|
|
XM_011528652.2:c.3874G>T
|
XP_011526954.1:p.Ala1292Ser
|
|
|
XM_017027704.1:c.3874G>T
|
XP_016883193.1:p.Ala1292Ser
|
|
|
XM_017027705.1:c.3874G>T
|
XP_016883194.1:p.Ala1292Ser
|
|
|
XM_017027706.1:c.3805G>T
|
XP_016883195.1:p.Ala1269Ser
|
|
|
NM_015338.6:c.3958G>T
MANE Select
|
NP_056153.2:p.Ala1320Ser
|
|
