ENST00000391944.8:c.2187C>T
|
ENSP00000375808.4:p.His729=
|
|
ENST00000682414.1:c.2187C>T
|
ENSP00000507019.1:p.His729=
|
|
ENST00000682508.1:n.2216C>T
|
|
|
ENST00000684218.1:c.*1445C>T
|
ENSP00000507804.1:n.*1445C>T
|
|
ENST00000684264.1:n.1743C>T
|
|
|
ENST00000684407.1:c.2064C>T
|
ENSP00000507775.1:p.His688=
|
|
ENST00000684458.1:c.*673C>T
|
ENSP00000508260.1:n.*673C>T
|
|
ENST00000684468.1:n.1899C>T
|
|
|
ENST00000391945.10:c.2187C>T
MANE Select
|
ENSP00000375809.4:p.His729=
|
|
ENST00000646507.1:n.2284C>T
|
|
|
ENST00000391941.6:c.2115C>T
|
ENSP00000375805.2:p.His705=
|
|
ENST00000391942.6:n.1358C>T
|
|
|
ENST00000391944.7:c.1953C>T
|
ENSP00000375808.3:p.His651=
|
|
ENST00000391945.8:c.2187C>T
|
ENSP00000375809.3:p.His729=
|
|
ENST00000588652.5:n.2275C>T
|
|
|
NM_000400.3:c.2187C>T , LRG_461t1:c.2187C>T
|
NP_000391.1:p.His729=
|
|
XM_011526611.1:c.2109C>T
|
XP_011524913.1:p.His703=
|
|
XM_011526611.2:c.2109C>T
|
XP_011524913.1:p.His703=
|
|
XM_017026467.1:c.2064C>T
|
XP_016881956.1:p.His688=
|
|
XR_001753633.2:n.2234C>T
|
|
|
XR_001753634.2:n.2170C>T
|
|
|
NM_000400.4:c.2187C>T
MANE Select
|
NP_000391.1:p.His729=
|
|