ENST00000391944.8:c.1836C>A
|
ENSP00000375808.4:p.His612Gln
|
|
ENST00000682414.1:c.1836C>A
|
ENSP00000507019.1:p.His612Gln
|
|
ENST00000682508.1:n.1865C>A
|
|
|
ENST00000684218.1:c.*1094C>A
|
ENSP00000507804.1:n.*1094C>A
|
|
ENST00000684264.1:n.1392C>A
|
|
|
ENST00000684407.1:c.1713C>A
|
ENSP00000507775.1:p.His571Gln
|
|
ENST00000684458.1:c.*322C>A
|
ENSP00000508260.1:n.*322C>A
|
|
ENST00000684468.1:n.1548C>A
|
|
|
ENST00000391945.10:c.1836C>A
MANE Select
|
ENSP00000375809.4:p.His612Gln
|
|
ENST00000646507.1:n.1933C>A
|
|
|
ENST00000391941.6:c.1764C>A
|
ENSP00000375805.2:p.His588Gln
|
|
ENST00000391942.6:n.1007C>A
|
|
|
ENST00000391944.7:c.1602C>A
|
ENSP00000375808.3:p.His534Gln
|
|
ENST00000391945.8:c.1836C>A
|
ENSP00000375809.3:p.His612Gln
|
|
ENST00000588652.5:n.1924C>A
|
|
|
NM_000400.3:c.1836C>A , LRG_461t1:c.1836C>A
|
NP_000391.1:p.His612Gln
|
|
XM_011526611.1:c.1758C>A
|
XP_011524913.1:p.His586Gln
|
|
XM_011526611.2:c.1758C>A
|
XP_011524913.1:p.His586Gln
|
|
XM_017026467.1:c.1713C>A
|
XP_016881956.1:p.His571Gln
|
|
XR_001753633.2:n.1883C>A
|
|
|
XR_001753634.2:n.1819C>A
|
|
|
NM_000400.4:c.1836C>A
MANE Select
|
NP_000391.1:p.His612Gln
|
|