ENST00000237596.7:c.1490T>G
MANE Select
|
ENSP00000237596.2:p.Ile497Ser
|
|
ENST00000237596.6:c.1490T>G
|
ENSP00000237596.2:p.Ile497Ser
|
|
ENST00000508588.5:c.-199+3355T>G
|
ENSP00000427131.1:n.-199+3355T>G
|
|
NM_000297.3:c.1490T>G
|
NP_000288.1:p.Ile497Ser
|
|
XM_011532028.1:c.1265T>G
|
XP_011530330.1:p.Ile422Ser
|
|
XM_011532029.1:c.770T>G
|
XP_011530331.1:p.Ile257Ser
|
|
XM_011532030.1:c.650T>G
|
XP_011530332.1:p.Ile217Ser
|
|
XR_244632.2:n.1585T>G
|
|
|
NR_156488.1:n.1577T>G
|
|
|
XM_011532028.2:c.1265T>G
|
XP_011530330.1:p.Ile422Ser
|
|
XM_011532030.2:c.650T>G
|
XP_011530332.1:p.Ile217Ser
|
|
NM_000297.4:c.1490T>G
MANE Select
|
NP_000288.1:p.Ile497Ser
|
|
NR_156488.2:n.1589T>G
|
|
|