ENST00000262493.12:c.1008C>G
MANE Select
|
ENSP00000262493.6:p.Phe336Leu
|
|
ENST00000562316.6:c.545-1107C>G
|
ENSP00000457238.2:n.545-1107C>G
|
|
ENST00000564727.2:c.303+9C>G
|
ENSP00000454971.2:n.303+9C>G
|
|
ENST00000568375.2:c.246C>G
|
|
|
ENST00000638210.1:n.1308C>G
|
|
|
ENST00000638705.1:c.1008C>G
|
ENSP00000491223.1:p.Phe336Leu
|
|
ENST00000638836.1:n.918C>G
|
|
|
ENST00000639251.1:n.909C>G
|
|
|
ENST00000639268.1:c.643C>G
|
|
|
ENST00000639341.1:c.533C>G
|
|
|
ENST00000639770.1:c.1046C>G
|
ENSP00000491999.1:n.1046C>G
|
|
ENST00000640390.1:n.938C>G
|
|
|
ENST00000640469.1:c.372C>G
|
ENSP00000491875.1:p.Phe124Leu
|
|
ENST00000640560.1:n.784C>G
|
|
|
ENST00000640893.1:c.*406C>G
|
ENSP00000492677.1:n.*406C>G
|
|
ENST00000262493.10:c.1008C>G
|
ENSP00000262493.6:p.Phe336Leu
|
|
ENST00000564727.1:c.228C>G
|
ENSP00000454971.1:p.Phe76Leu
|
|
ENST00000568375.1:n.246C>G
|
|
|
NM_020988.2:c.1008C>G
|
NP_066268.1:p.Phe336Leu
|
|
XM_011523003.1:c.882C>G
|
XP_011521305.1:p.Phe294Leu
|
|
XM_011523003.3:c.882C>G
|
XP_011521305.1:p.Phe294Leu
|
|
NM_020988.3:c.1008C>G
MANE Select
|
NP_066268.1:p.Phe336Leu
|
|