ENST00000262493.12:c.850T>G
MANE Select
|
ENSP00000262493.6:p.Leu284Val
|
|
ENST00000562316.6:c.517T>G
|
ENSP00000457238.2:p.Leu173Val
|
|
ENST00000564727.2:c.154T>G
|
ENSP00000454971.2:p.Leu52Val
|
|
ENST00000568375.2:c.116-3356T>G
|
|
|
ENST00000638185.1:n.1065T>G
|
|
|
ENST00000638210.1:n.1150T>G
|
|
|
ENST00000638705.1:c.850T>G
|
ENSP00000491223.1:p.Leu284Val
|
|
ENST00000638836.1:n.760T>G
|
|
|
ENST00000639055.1:n.1571T>G
|
|
|
ENST00000639251.1:n.751T>G
|
|
|
ENST00000639268.1:c.485T>G
|
|
|
ENST00000639341.1:c.375T>G
|
|
|
ENST00000639770.1:c.888T>G
|
ENSP00000491999.1:n.888T>G
|
|
ENST00000640390.1:n.780T>G
|
|
|
ENST00000640469.1:c.214T>G
|
ENSP00000491875.1:p.Leu72Val
|
|
ENST00000640560.1:n.626T>G
|
|
|
ENST00000640893.1:c.*248T>G
|
ENSP00000492677.1:n.*248T>G
|
|
ENST00000262493.10:c.850T>G
|
ENSP00000262493.6:p.Leu284Val
|
|
ENST00000564727.1:c.70T>G
|
ENSP00000454971.1:p.Leu24Val
|
|
ENST00000568375.1:n.116-3356T>G
|
|
|
NM_020988.2:c.850T>G
|
NP_066268.1:p.Leu284Val
|
|
XM_011523003.1:c.724T>G
|
XP_011521305.1:p.Leu242Val
|
|
XM_011523003.3:c.724T>G
|
XP_011521305.1:p.Leu242Val
|
|
NM_020988.3:c.850T>G
MANE Select
|
NP_066268.1:p.Leu284Val
|
|