ENST00000639857.2:c.*683C>T
|
ENSP00000491593.2:n.*683C>T
|
|
ENST00000685487.1:c.*1724C>T
|
ENSP00000508503.1:n.*1724C>T
|
|
ENST00000687120.1:n.4343C>T
|
|
|
ENST00000687906.1:c.*740C>T
|
ENSP00000509536.1:n.*740C>T
|
|
ENST00000688597.1:c.*740C>T
|
ENSP00000510628.1:n.*740C>T
|
|
ENST00000688701.1:n.1766C>T
|
|
|
ENST00000690210.1:c.*740C>T
|
ENSP00000509272.1:n.*740C>T
|
|
ENST00000690472.1:n.1731C>T
|
|
|
ENST00000692624.1:c.*1068C>T
|
ENSP00000508953.1:n.*1068C>T
|
|
ENST00000351677.7:c.*740C>T
MANE Select
|
ENSP00000340944.3:n.*740C>T
|
|
ENST00000351677.6:c.*740C>T
|
ENSP00000340944.2:n.*740C>T
|
|
NM_002834.3:c.*740C>T , LRG_614t1:c.*740C>T
|
NP_002825.3:n.*740C>T
|
|
XM_006719526.1:c.*740C>T
|
XP_006719589.1:n.*740C>T
|
|
XM_006719527.1:c.*740C>T
|
XP_006719590.1:n.*740C>T
|
|
XM_011538613.1:c.*740C>T
|
XP_011536915.1:n.*740C>T
|
|
NM_001330437.1:c.*740C>T
|
NP_001317366.1:n.*740C>T
|
|
NM_002834.4:c.*740C>T
|
NP_002825.3:n.*740C>T
|
|
XM_011538613.2:c.*740C>T
|
XP_011536915.1:n.*740C>T
|
|
XM_017019722.1:c.*740C>T
|
XP_016875211.1:n.*740C>T
|
|
NM_001330437.2:c.*740C>T
|
NP_001317366.1:n.*740C>T
|
|
NM_001374625.1:c.*740C>T
|
NP_001361554.1:n.*740C>T
|
|
NM_002834.5:c.*740C>T
MANE Select
|
NP_002825.3:n.*740C>T
|
|