ENST00000683572.1:n.760T>G
|
|
|
ENST00000341947.7:c.4954T>G
MANE Select
|
ENSP00000339915.2:p.Ser1652Ala
|
|
ENST00000341947.6:c.4954T>G
|
ENSP00000339915.2:p.Ser1652Ala
|
|
ENST00000361917.5:c.4633T>G
|
ENSP00000355123.1:p.Ser1545Ala
|
|
ENST00000374708.8:c.4696T>G
|
ENSP00000363840.4:p.Ser1566Ala
|
|
ENST00000477772.1:n.744T>G
|
|
|
NM_080679.2:c.4633T>G
|
NP_542410.2:p.Ser1545Ala
|
|
NM_080680.2:c.4954T>G
|
NP_542411.2:p.Ser1652Ala
|
|
NM_080681.2:c.4696T>G
|
NP_542412.2:p.Ser1566Ala
|
|
XM_011514298.1:c.4108T>G
|
XP_011512600.1:p.Ser1370Ala
|
|
XM_011514299.1:c.4240T>G
|
XP_011512601.1:p.Ser1414Ala
|
|
XM_011514300.1:c.4060T>G
|
XP_011512602.1:p.Ser1354Ala
|
|
XM_011514301.1:c.3997T>G
|
XP_011512603.1:p.Ser1333Ala
|
|
XM_011514302.1:c.3841T>G
|
XP_011512604.1:p.Ser1281Ala
|
|
XM_011514299.2:c.4240T>G
|
XP_011512601.1:p.Ser1414Ala
|
|
XM_011514300.2:c.4060T>G
|
XP_011512602.1:p.Ser1354Ala
|
|
XM_011514302.2:c.3841T>G
|
XP_011512604.1:p.Ser1281Ala
|
|
XM_017010250.1:c.4954T>G
|
XP_016865739.1:p.Ser1652Ala
|
|
XM_017010251.2:c.3772T>G
|
XP_016865740.1:p.Ser1258Ala
|
|
NM_080680.3:c.4954T>G
MANE Select
|
NP_542411.2:p.Ser1652Ala
|
|
NM_080681.3:c.4696T>G
|
NP_542412.2:p.Ser1566Ala
|
|
NM_080679.3:c.4633T>G
|
NP_542410.2:p.Ser1545Ala
|
|