ENST00000237596.7:c.1023T>G
MANE Select
|
ENSP00000237596.2:p.Ile341Met
|
|
ENST00000237596.6:c.1023T>G
|
ENSP00000237596.2:p.Ile341Met
|
|
ENST00000506367.1:n.470T>G
|
|
|
NM_000297.3:c.1023T>G
|
NP_000288.1:p.Ile341Met
|
|
XM_011532028.1:c.1023T>G
|
XP_011530330.1:p.Ile341Met
|
|
XM_011532029.1:c.303T>G
|
XP_011530331.1:p.Ile101Met
|
|
XM_011532030.1:c.183T>G
|
XP_011530332.1:p.Ile61Met
|
|
XR_244632.2:n.1118T>G
|
|
|
NR_156488.1:n.1110T>G
|
|
|
XM_011532028.2:c.1023T>G
|
XP_011530330.1:p.Ile341Met
|
|
XM_011532030.2:c.183T>G
|
XP_011530332.1:p.Ile61Met
|
|
NM_000297.4:c.1023T>G
MANE Select
|
NP_000288.1:p.Ile341Met
|
|
NR_156488.2:n.1122T>G
|
|
|