ENST00000355699.7:c.1351G>T
MANE Select
|
ENSP00000347927.2:p.Ala451Ser
|
|
ENST00000355699.6:c.1351G>T
|
ENSP00000347927.2:p.Ala451Ser
|
|
ENST00000356589.6:c.1258G>T
|
ENSP00000348997.2:p.Ala420Ser
|
|
ENST00000371916.5:c.607G>T
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ENSP00000360984.2:p.Ala203Ser
|
|
ENST00000371929.7:c.1351G>T
|
ENSP00000360997.3:p.Ala451Ser
|
|
ENST00000474918.1:c.*155G>T
|
ENSP00000435305.1:n.*155G>T
|
|
ENST00000485925.5:n.974-2495G>T
|
|
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ENST00000495234.5:c.*635G>T
|
ENSP00000435274.1:n.*635G>T
|
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NM_139025.4:c.1351G>T , LRG_544t1:c.1351G>T
|
NP_620594.1:p.Ala451Ser
|
|
NM_139026.4:c.1258G>T
|
NP_620595.1:p.Ala420Ser
|
|
NM_139027.4:c.1351G>T
|
NP_620596.2:p.Ala451Ser
|
|
NR_024514.2:n.993-2495G>T
|
|
|
XM_011518174.1:c.961G>T
|
XP_011516476.1:p.Ala321Ser
|
|
XM_011518175.1:c.1351G>T
|
XP_011516477.1:p.Ala451Ser
|
|
XM_011518176.1:c.367G>T
|
XP_011516478.1:p.Ala123Ser
|
|
XM_011518177.1:c.361G>T
|
XP_011516479.1:p.Ala121Ser
|
|
XM_011518178.1:c.16G>T
|
XP_011516480.1:p.Ala6Ser
|
|
XM_011518179.1:c.137G>T
|
XP_011516481.1:p.Arg46Leu
|
|
XM_011518180.1:c.687-7992G>T
|
XP_011516482.1:n.687-7992G>T
|
|
XM_011518176.3:c.367G>T
|
XP_011516478.1:p.Ala123Ser
|
|
XM_011518178.2:c.16G>T
|
XP_011516480.1:p.Ala6Ser
|
|
XM_017014232.1:c.1339G>T
|
XP_016869721.1:p.Ala447Ser
|
|
XM_017014233.1:c.961G>T
|
XP_016869722.1:p.Ala321Ser
|
|
XM_017014234.2:c.361G>T
|
XP_016869723.1:p.Ala121Ser
|
|
XM_017014235.1:c.1351G>T
|
XP_016869724.1:p.Ala451Ser
|
|
XR_001746171.1:n.2576G>T
|
|
|
NM_139026.5:c.1258G>T
|
NP_620595.1:p.Ala420Ser
|
|
NM_139027.5:c.1351G>T
|
NP_620596.2:p.Ala451Ser
|
|
NM_139025.5:c.1351G>T
|
NP_620594.1:p.Ala451Ser
|
|
NM_139026.6:c.1258G>T
|
NP_620595.1:p.Ala420Ser
|
|
NM_139027.6:c.1351G>T
MANE Select
|
NP_620596.2:p.Ala451Ser
|
|
NR_024514.3:n.995-2495G>T
|
|
|