ENST00000254108.12:c.924T>C
MANE Select
|
ENSP00000254108.8:p.Ile308=
|
|
ENST00000254108.11:c.924T>C
|
ENSP00000254108.7:p.Ile308=
|
|
ENST00000380244.7:c.921T>C
|
ENSP00000369594.3:p.Ile307=
|
|
ENST00000474990.5:n.218T>C
|
|
|
ENST00000487509.6:n.4099T>C
|
|
|
ENST00000564766.1:n.748T>C
|
|
|
ENST00000566605.5:c.*97T>C
|
ENSP00000455073.1:n.*97T>C
|
|
ENST00000568685.1:c.927T>C
|
ENSP00000455282.1:p.Ile309=
|
|
ENST00000568901.2:n.298T>C
|
|
|
NM_001170634.1:c.921T>C
|
NP_001164105.1:p.Ile307=
|
|
NM_001170937.1:c.912T>C
|
NP_001164408.1:p.Ile304=
|
|
NM_004960.3:c.924T>C , LRG_655t1:c.924T>C
|
NP_004951.1:p.Ile308=
|
|
NR_028388.2:n.994T>C
|
|
|
XM_005255233.3:c.309T>C
|
XP_005255290.1:p.Ile103=
|
|
XM_011545781.1:c.918T>C
|
XP_011544083.1:p.Ile306=
|
|
XM_011545782.1:c.309T>C
|
XP_011544084.1:p.Ile103=
|
|
XM_005255233.5:c.309T>C
|
XP_005255290.1:p.Ile103=
|
|
XM_011545782.2:c.309T>C
|
XP_011544084.1:p.Ile103=
|
|
XM_024450221.1:c.915T>C
|
XP_024305989.1:p.Ile305=
|
|
NM_004960.4:c.924T>C
MANE Select
|
NP_004951.1:p.Ile308=
|
|