ENST00000299314.12:c.3213T>G
MANE Select
|
ENSP00000299314.7:p.Ile1071Met
|
|
ENST00000299314.11:c.3213T>G
|
ENSP00000299314.7:p.Ile1071Met
|
|
ENST00000549194.1:n.79T>G
|
|
|
ENST00000550718.1:c.25T>G
|
|
|
NM_024312.4:c.3213T>G
|
NP_077288.2:p.Ile1071Met
|
|
XM_006719593.2:c.3213T>G
|
XP_006719656.1:p.Ile1071Met
|
|
XM_011538731.1:c.3132T>G
|
XP_011537033.1:p.Ile1044Met
|
|
XM_006719593.3:c.3213T>G
|
XP_006719656.1:p.Ile1071Met
|
|
XM_011538731.2:c.3132T>G
|
XP_011537033.1:p.Ile1044Met
|
|
XM_017019961.1:c.2997T>G
|
XP_016875450.1:p.Ile999Met
|
|
XM_017019962.2:c.1986T>G
|
XP_016875451.1:p.Ile662Met
|
|
NM_024312.5:c.3213T>G
MANE Select
|
NP_077288.2:p.Ile1071Met
|
|