ENST00000029410.10:c.371T>G
MANE Select
|
ENSP00000029410.5:p.Ile124Ser
|
|
ENST00000029410.9:c.371T>G
|
ENSP00000029410.5:p.Ile124Ser
|
|
ENST00000502420.1:n.350T>G
|
|
|
ENST00000505433.5:c.371T>G
|
ENSP00000425591.1:p.Ile124Ser
|
|
ENST00000505468.1:c.29T>G
|
ENSP00000420886.1:p.Ile10Ser
|
|
ENST00000507061.1:c.188T>G
|
ENSP00000423868.1:p.Ile63Ser
|
|
ENST00000510761.1:c.29T>G
|
ENSP00000423438.1:p.Ile10Ser
|
|
NM_007255.2:c.371T>G
|
NP_009186.1:p.Ile124Ser
|
|
XM_005265805.2:c.29T>G
|
XP_005265862.1:p.Ile10Ser
|
|
XM_006714816.2:c.-129T>G
|
XP_006714879.1:n.-129T>G
|
|
XM_011534421.1:c.29T>G
|
XP_011532723.1:p.Ile10Ser
|
|
XM_006714816.4:c.-129T>G
|
XP_006714879.1:n.-129T>G
|
|
XM_017008999.2:c.29T>G
|
XP_016864488.1:p.Ile10Ser
|
|
NM_007255.3:c.371T>G
MANE Select
|
NP_009186.1:p.Ile124Ser
|
|