ENST00000299314.12:c.2823T>G
MANE Select
|
ENSP00000299314.7:p.Ile941Met
|
|
ENST00000299314.11:c.2823T>G
|
ENSP00000299314.7:p.Ile941Met
|
|
NM_024312.4:c.2823T>G
|
NP_077288.2:p.Ile941Met
|
|
XM_006719593.2:c.2823T>G
|
XP_006719656.1:p.Ile941Met
|
|
XM_011538731.1:c.2742T>G
|
XP_011537033.1:p.Ile914Met
|
|
XM_006719593.3:c.2823T>G
|
XP_006719656.1:p.Ile941Met
|
|
XM_011538731.2:c.2742T>G
|
XP_011537033.1:p.Ile914Met
|
|
XM_017019961.1:c.2607T>G
|
XP_016875450.1:p.Ile869Met
|
|
XM_017019962.2:c.1596T>G
|
XP_016875451.1:p.Ile532Met
|
|
NM_024312.5:c.2823T>G
MANE Select
|
NP_077288.2:p.Ile941Met
|
|