ENST00000391944.8:c.1446C>T
|
ENSP00000375808.4:p.Thr482=
|
|
ENST00000682414.1:c.1446C>T
|
ENSP00000507019.1:p.Thr482=
|
|
ENST00000682508.1:n.1475C>T
|
|
|
ENST00000684218.1:c.*704C>T
|
ENSP00000507804.1:n.*704C>T
|
|
ENST00000684264.1:n.1002C>T
|
|
|
ENST00000684407.1:c.1323C>T
|
ENSP00000507775.1:p.Thr441=
|
|
ENST00000684458.1:c.1376C>T
|
ENSP00000508260.1:p.Pro459Leu
|
|
ENST00000684468.1:n.1222C>T
|
|
|
ENST00000391945.10:c.1446C>T
MANE Select
|
ENSP00000375809.4:p.Thr482=
|
|
ENST00000587376.6:c.569C>T
|
|
|
ENST00000646507.1:n.1543C>T
|
|
|
ENST00000391941.6:c.1374C>T
|
ENSP00000375805.2:p.Thr458=
|
|
ENST00000391942.6:n.617C>T
|
|
|
ENST00000391944.7:c.1212C>T
|
ENSP00000375808.3:p.Thr404=
|
|
ENST00000391945.8:c.1446C>T
|
ENSP00000375809.3:p.Thr482=
|
|
ENST00000587376.5:c.569C>T
|
|
|
ENST00000588652.5:n.1534C>T
|
|
|
NM_000400.3:c.1446C>T , LRG_461t1:c.1446C>T
|
NP_000391.1:p.Thr482=
|
|
XM_011526611.1:c.1368C>T
|
XP_011524913.1:p.Thr456=
|
|
XR_935763.1:n.1493C>T
|
|
|
XM_011526611.2:c.1368C>T
|
XP_011524913.1:p.Thr456=
|
|
XM_017026467.1:c.1323C>T
|
XP_016881956.1:p.Thr441=
|
|
XR_001753633.2:n.1493C>T
|
|
|
XR_001753634.2:n.1493C>T
|
|
|
NM_000400.4:c.1446C>T
MANE Select
|
NP_000391.1:p.Thr482=
|
|