ENST00000262493.12:c.845C>G
MANE Select
|
ENSP00000262493.6:p.Ser282Ter
|
|
ENST00000562316.6:c.512C>G
|
ENSP00000457238.2:p.Ser171Ter
|
|
ENST00000564727.2:c.149C>G
|
ENSP00000454971.2:p.Ser50Ter
|
|
ENST00000568375.2:c.116-3361C>G
|
|
|
ENST00000638185.1:n.1060C>G
|
|
|
ENST00000638210.1:n.1145C>G
|
|
|
ENST00000638705.1:c.845C>G
|
ENSP00000491223.1:p.Ser282Ter
|
|
ENST00000638836.1:n.755C>G
|
|
|
ENST00000639055.1:n.1566C>G
|
|
|
ENST00000639251.1:n.746C>G
|
|
|
ENST00000639268.1:c.480C>G
|
|
|
ENST00000639341.1:c.370C>G
|
|
|
ENST00000639770.1:c.883C>G
|
ENSP00000491999.1:n.883C>G
|
|
ENST00000640390.1:n.775C>G
|
|
|
ENST00000640469.1:c.209C>G
|
ENSP00000491875.1:p.Ser70Ter
|
|
ENST00000640560.1:n.621C>G
|
|
|
ENST00000640893.1:c.*243C>G
|
ENSP00000492677.1:n.*243C>G
|
|
ENST00000262493.10:c.845C>G
|
ENSP00000262493.6:p.Ser282Ter
|
|
ENST00000564727.1:c.65C>G
|
ENSP00000454971.1:p.Ser22Ter
|
|
ENST00000568375.1:n.116-3361C>G
|
|
|
NM_020988.2:c.845C>G
|
NP_066268.1:p.Ser282Ter
|
|
XM_011523003.1:c.719C>G
|
XP_011521305.1:p.Ser240Ter
|
|
XM_011523003.3:c.719C>G
|
XP_011521305.1:p.Ser240Ter
|
|
NM_020988.3:c.845C>G
MANE Select
|
NP_066268.1:p.Ser282Ter
|
|