ENST00000322776.11:c.1156C>A
MANE Select
|
ENSP00000322450.6:p.Arg386Ser
|
|
ENST00000647561.1:c.1156C>A
|
ENSP00000497587.1:p.Arg386Ser
|
|
ENST00000322776.10:c.1156C>A
|
ENSP00000322450.6:p.Arg386Ser
|
|
ENST00000415352.6:c.1135C>A
|
ENSP00000395368.2:p.Arg379Ser
|
|
ENST00000526770.5:n.1439C>A
|
|
|
ENST00000527355.5:c.370-148C>A
|
ENSP00000432637.1:n.370-148C>A
|
|
ENST00000527923.1:n.498C>A
|
|
|
ENST00000529927.5:c.1129C>A
|
ENSP00000436766.1:p.Arg377Ser
|
|
ENST00000531250.1:n.420C>A
|
|
|
ENST00000532303.5:c.853C>A
|
ENSP00000432015.1:p.Arg285Ser
|
|
ENST00000533919.5:c.560C>A
|
ENSP00000435199.1:n.560C>A
|
|
ENST00000534352.1:n.254C>A
|
|
|
NM_001166102.1:c.1129C>A
|
NP_001159574.1:p.Arg377Ser
|
|
NM_007103.3:c.1156C>A
|
NP_009034.2:p.Arg386Ser
|
|
NM_001166102.2:c.1129C>A
|
NP_001159574.1:p.Arg377Ser
|
|
NM_007103.4:c.1156C>A
MANE Select
|
NP_009034.2:p.Arg386Ser
|
|