ENST00000391944.8:c.1856T>A
|
ENSP00000375808.4:p.Ile619Asn
|
|
ENST00000682414.1:c.1856T>A
|
ENSP00000507019.1:p.Ile619Asn
|
|
ENST00000682508.1:n.1885T>A
|
|
|
ENST00000684218.1:c.*1114T>A
|
ENSP00000507804.1:n.*1114T>A
|
|
ENST00000684264.1:n.1412T>A
|
|
|
ENST00000684407.1:c.1733T>A
|
ENSP00000507775.1:p.Ile578Asn
|
|
ENST00000684458.1:c.*342T>A
|
ENSP00000508260.1:n.*342T>A
|
|
ENST00000684468.1:n.1568T>A
|
|
|
ENST00000391945.10:c.1856T>A
MANE Select
|
ENSP00000375809.4:p.Ile619Asn
|
|
ENST00000646507.1:n.1953T>A
|
|
|
ENST00000391941.6:c.1784T>A
|
ENSP00000375805.2:p.Ile595Asn
|
|
ENST00000391942.6:n.1027T>A
|
|
|
ENST00000391944.7:c.1622T>A
|
ENSP00000375808.3:p.Ile541Asn
|
|
ENST00000391945.8:c.1856T>A
|
ENSP00000375809.3:p.Ile619Asn
|
|
ENST00000588652.5:n.1944T>A
|
|
|
NM_000400.3:c.1856T>A , LRG_461t1:c.1856T>A
|
NP_000391.1:p.Ile619Asn
|
|
XM_011526611.1:c.1778T>A
|
XP_011524913.1:p.Ile593Asn
|
|
XM_011526611.2:c.1778T>A
|
XP_011524913.1:p.Ile593Asn
|
|
XM_017026467.1:c.1733T>A
|
XP_016881956.1:p.Ile578Asn
|
|
XR_001753633.2:n.1903T>A
|
|
|
XR_001753634.2:n.1839T>A
|
|
|
NM_000400.4:c.1856T>A
MANE Select
|
NP_000391.1:p.Ile619Asn
|
|