ENST00000395925.8:c.582T>A
MANE Select
|
ENSP00000379258.3:p.His194Gln
|
|
ENST00000677288.1:c.405T>A
|
ENSP00000503986.1:p.His135Gln
|
|
ENST00000677605.1:c.582T>A
|
ENSP00000503743.1:p.His194Gln
|
|
ENST00000678429.1:c.582T>A
|
ENSP00000502957.1:p.His194Gln
|
|
ENST00000395925.7:c.582T>A
|
ENSP00000379258.3:p.His194Gln
|
|
ENST00000479210.1:n.559T>A
|
|
|
NM_000168.5:c.582T>A
|
NP_000159.3:p.His194Gln
|
|
XM_005249703.1:c.582T>A
|
XP_005249760.1:p.His194Gln
|
|
XM_005249704.2:c.582T>A
|
XP_005249761.1:p.His194Gln
|
|
XM_011515272.1:c.582T>A
|
XP_011513574.1:p.His194Gln
|
|
XM_011515273.1:c.582T>A
|
XP_011513575.1:p.His194Gln
|
|
XM_011515274.1:c.405T>A
|
XP_011513576.1:p.His135Gln
|
|
XM_011515274.2:c.405T>A
|
XP_011513576.1:p.His135Gln
|
|
XM_017011997.1:c.579T>A
|
XP_016867486.1:p.His193Gln
|
|
NM_000168.6:c.582T>A
MANE Select
|
NP_000159.3:p.His194Gln
|
|