ENST00000281928.9:c.2679A>G
MANE Select
|
ENSP00000281928.3:p.Thr893=
|
|
ENST00000548743.2:c.2649A>G
|
ENSP00000448553.2:p.Thr883=
|
|
ENST00000549786.2:c.2107A>G
|
|
|
ENST00000647927.1:n.3052A>G
|
|
|
ENST00000648173.1:n.1474A>G
|
|
|
ENST00000648379.1:n.1047A>G
|
|
|
ENST00000648737.1:n.2443A>G
|
|
|
ENST00000648916.1:n.690A>G
|
|
|
ENST00000649607.1:c.863A>G
|
|
|
ENST00000650226.1:c.2679A>G
|
ENSP00000496981.1:p.Thr893=
|
|
ENST00000281928.7:c.2679A>G
|
ENSP00000281928.3:p.Thr893=
|
|
NM_015335.4:c.2679A>G
|
NP_056150.1:p.Thr893=
|
|
XM_011538080.1:c.2679A>G
|
XP_011536382.1:p.Thr893=
|
|
XM_011538081.1:c.2676A>G
|
XP_011536383.1:p.Thr892=
|
|
XM_011538082.1:c.2649A>G
|
XP_011536384.1:p.Thr883=
|
|
XM_011538080.2:c.2679A>G
|
XP_011536382.1:p.Thr893=
|
|
XM_011538081.2:c.2676A>G
|
XP_011536383.1:p.Thr892=
|
|
XM_011538082.2:c.2649A>G
|
XP_011536384.1:p.Thr883=
|
|
XM_017019090.1:c.2676A>G
|
XP_016874579.1:p.Thr892=
|
|
NM_015335.5:c.2679A>G
MANE Select
|
NP_056150.1:p.Thr893=
|
|