ENST00000262493.12:c.1019C>G
MANE Select
|
ENSP00000262493.6:p.Thr340Ser
|
|
ENST00000562316.6:c.545-1096C>G
|
ENSP00000457238.2:n.545-1096C>G
|
|
ENST00000564727.2:c.303+20C>G
|
ENSP00000454971.2:n.303+20C>G
|
|
ENST00000568375.2:c.257C>G
|
|
|
ENST00000638210.1:n.1319C>G
|
|
|
ENST00000638705.1:c.1019C>G
|
ENSP00000491223.1:p.Thr340Ser
|
|
ENST00000638836.1:n.929C>G
|
|
|
ENST00000639251.1:n.920C>G
|
|
|
ENST00000639268.1:c.654C>G
|
|
|
ENST00000639341.1:c.544C>G
|
|
|
ENST00000639770.1:c.1057C>G
|
ENSP00000491999.1:n.1057C>G
|
|
ENST00000640390.1:n.949C>G
|
|
|
ENST00000640469.1:c.383C>G
|
ENSP00000491875.1:p.Thr128Ser
|
|
ENST00000640560.1:n.795C>G
|
|
|
ENST00000640893.1:c.*417C>G
|
ENSP00000492677.1:n.*417C>G
|
|
ENST00000262493.10:c.1019C>G
|
ENSP00000262493.6:p.Thr340Ser
|
|
ENST00000564727.1:c.239C>G
|
ENSP00000454971.1:p.Thr80Ser
|
|
ENST00000568375.1:n.257C>G
|
|
|
NM_020988.2:c.1019C>G
|
NP_066268.1:p.Thr340Ser
|
|
XM_011523003.1:c.893C>G
|
XP_011521305.1:p.Thr298Ser
|
|
XM_011523003.3:c.893C>G
|
XP_011521305.1:p.Thr298Ser
|
|
NM_020988.3:c.1019C>G
MANE Select
|
NP_066268.1:p.Thr340Ser
|
|