ENST00000237596.7:c.1355T>G
MANE Select
|
ENSP00000237596.2:p.Ile452Ser
|
|
ENST00000237596.6:c.1355T>G
|
ENSP00000237596.2:p.Ile452Ser
|
|
ENST00000508588.5:c.-199+3220T>G
|
ENSP00000427131.1:n.-199+3220T>G
|
|
NM_000297.3:c.1355T>G
|
NP_000288.1:p.Ile452Ser
|
|
XM_011532028.1:c.1130T>G
|
XP_011530330.1:p.Ile377Ser
|
|
XM_011532029.1:c.635T>G
|
XP_011530331.1:p.Ile212Ser
|
|
XM_011532030.1:c.515T>G
|
XP_011530332.1:p.Ile172Ser
|
|
XR_244632.2:n.1450T>G
|
|
|
NR_156488.1:n.1442T>G
|
|
|
XM_011532028.2:c.1130T>G
|
XP_011530330.1:p.Ile377Ser
|
|
XM_011532030.2:c.515T>G
|
XP_011530332.1:p.Ile172Ser
|
|
NM_000297.4:c.1355T>G
MANE Select
|
NP_000288.1:p.Ile452Ser
|
|
NR_156488.2:n.1454T>G
|
|
|