ENST00000262367.10:c.5192A>T
MANE Select
|
ENSP00000262367.5:p.Asn1731Ile
|
|
ENST00000262367.9:c.5192A>T
|
ENSP00000262367.5:p.Asn1731Ile
|
|
ENST00000382070.7:c.5078A>T
|
ENSP00000371502.3:p.Asn1693Ile
|
|
NM_001079846.1:c.5078A>T
|
NP_001073315.1:p.Asn1693Ile
|
|
NM_004380.2:c.5192A>T
|
NP_004371.2:p.Asn1731Ile
|
|
XM_005255124.3:c.5147A>T
|
XP_005255181.1:p.Asn1716Ile
|
|
XM_005255125.3:c.4775A>T
|
XP_005255182.1:p.Asn1592Ile
|
|
XM_006720848.2:c.4931A>T
|
XP_006720911.1:p.Asn1644Ile
|
|
XM_011522380.1:c.5138A>T
|
XP_011520682.1:p.Asn1713Ile
|
|
XM_011522381.1:c.4439A>T
|
XP_011520683.1:p.Asn1480Ile
|
|
XM_005255124.4:c.5147A>T
|
XP_005255181.1:p.Asn1716Ile
|
|
XM_005255125.4:c.4775A>T
|
XP_005255182.1:p.Asn1592Ile
|
|
XM_006720848.3:c.4931A>T
|
XP_006720911.1:p.Asn1644Ile
|
|
XM_011522381.2:c.4439A>T
|
XP_011520683.1:p.Asn1480Ile
|
|
XM_017022944.1:c.5186A>T
|
XP_016878433.1:p.Asn1729Ile
|
|
NM_004380.3:c.5192A>T
MANE Select
|
NP_004371.2:p.Asn1731Ile
|
|