ENST00000237596.7:c.1356T>G
MANE Select
|
ENSP00000237596.2:p.Ile452Met
|
|
ENST00000237596.6:c.1356T>G
|
ENSP00000237596.2:p.Ile452Met
|
|
ENST00000508588.5:c.-199+3221T>G
|
ENSP00000427131.1:n.-199+3221T>G
|
|
NM_000297.3:c.1356T>G
|
NP_000288.1:p.Ile452Met
|
|
XM_011532028.1:c.1131T>G
|
XP_011530330.1:p.Ile377Met
|
|
XM_011532029.1:c.636T>G
|
XP_011530331.1:p.Ile212Met
|
|
XM_011532030.1:c.516T>G
|
XP_011530332.1:p.Ile172Met
|
|
XR_244632.2:n.1451T>G
|
|
|
NR_156488.1:n.1443T>G
|
|
|
XM_011532028.2:c.1131T>G
|
XP_011530330.1:p.Ile377Met
|
|
XM_011532030.2:c.516T>G
|
XP_011530332.1:p.Ile172Met
|
|
NM_000297.4:c.1356T>G
MANE Select
|
NP_000288.1:p.Ile452Met
|
|
NR_156488.2:n.1455T>G
|
|
|