|
ENST00000407991.3:c.836T>A
MANE Select
|
ENSP00000385026.1:p.Ile279Asn
|
|
|
ENST00000637241.1:c.*666T>A
|
ENSP00000490690.1:n.*666T>A
|
|
|
ENST00000240132.7:c.791T>A
|
ENSP00000240132.2:p.Ile264Asn
|
|
|
ENST00000407991.2:c.836T>A
|
ENSP00000385026.1:p.Ile279Asn
|
|
|
ENST00000520600.1:n.290-1853T>A
|
|
|
|
ENST00000520933.7:c.770T>A
|
ENSP00000429616.2:p.Ile257Asn
|
|
|
ENST00000523695.5:c.*238T>A
|
ENSP00000430612.1:n.*238T>A
|
|
|
NM_000742.3:c.836T>A
|
NP_000733.2:p.Ile279Asn
|
|
|
NM_001282455.1:c.791T>A
|
NP_001269384.1:p.Ile264Asn
|
|
|
XM_005273397.1:c.359T>A
|
XP_005273454.1:p.Ile120Asn
|
|
|
XM_006716282.1:c.836T>A
|
XP_006716345.1:p.Ile279Asn
|
|
|
XM_011544388.1:c.836T>A
|
XP_011542690.1:p.Ile279Asn
|
|
|
XM_011544389.1:c.242T>A
|
XP_011542691.1:p.Ile81Asn
|
|
|
NM_001347705.1:c.359T>A
|
NP_001334634.1:p.Ile120Asn
|
|
|
NM_001347706.1:c.359T>A
|
NP_001334635.1:p.Ile120Asn
|
|
|
NM_001347707.1:c.242T>A
|
NP_001334636.1:p.Ile81Asn
|
|
|
NM_001347708.1:c.242T>A
|
NP_001334637.1:p.Ile81Asn
|
|
|
XM_011544389.2:c.242T>A
|
XP_011542691.1:p.Ile81Asn
|
|
|
NM_000742.4:c.836T>A
MANE Select
|
NP_000733.2:p.Ile279Asn
|
|
|
NM_001282455.2:c.791T>A
|
NP_001269384.1:p.Ile264Asn
|
|
|
NM_001347705.2:c.359T>A
|
NP_001334634.1:p.Ile120Asn
|
|
|
NM_001347706.2:c.359T>A
|
NP_001334635.1:p.Ile120Asn
|
|
|
NM_001347707.2:c.242T>A
|
NP_001334636.1:p.Ile81Asn
|
|
|
NM_001347708.2:c.242T>A
|
NP_001334637.1:p.Ile81Asn
|
|
