ENST00000318471.5:c.891G>T
MANE Select
|
ENSP00000315680.3:p.Gln297His
|
|
ENST00000541292.6:c.*156G>T
|
ENSP00000441004.1:n.*156G>T
|
|
ENST00000678002.1:c.579G>T
|
|
|
ENST00000678557.1:c.777G>T
|
ENSP00000502962.1:p.Gln259His
|
|
ENST00000679286.1:c.771G>T
|
ENSP00000503168.1:p.Gln257His
|
|
ENST00000318471.4:c.891G>T
|
ENSP00000315680.3:p.Gln297His
|
|
NM_000288.3:c.891G>T
|
NP_000279.1:p.Gln297His
|
|
XM_005267019.3:c.777G>T
|
XP_005267076.1:p.Gln259His
|
|
XM_006715502.1:c.597G>T
|
XP_006715565.1:p.Gln199His
|
|
XM_005267019.4:c.777G>T
|
XP_005267076.1:p.Gln259His
|
|
XM_006715502.2:c.597G>T
|
XP_006715565.1:p.Gln199His
|
|
XM_017010934.2:c.*14G>T
|
XP_016866423.1:n.*14G>T
|
|
NM_000288.4:c.891G>T
MANE Select
|
NP_000279.1:p.Gln297His
|
|