ENST00000697124.1:n.1377T>C
|
|
|
ENST00000219596.6:c.2256T>C
MANE Select
|
ENSP00000219596.1:p.Leu752=
|
|
ENST00000219596.5:c.2256T>C
|
ENSP00000219596.1:p.Leu752=
|
|
ENST00000339854.8:c.1716T>C
|
ENSP00000339639.4:p.Leu572=
|
|
ENST00000536379.5:c.1623T>C
|
ENSP00000445079.1:p.Leu541=
|
|
ENST00000536980.5:c.*532T>C
|
ENSP00000444178.1:n.*532T>C
|
|
ENST00000537682.5:c.*532T>C
|
ENSP00000438611.1:n.*532T>C
|
|
ENST00000538326.5:c.*881T>C
|
ENSP00000437486.1:n.*881T>C
|
|
ENST00000539145.5:c.1177T>C
|
ENSP00000444471.1:n.1177T>C
|
|
ENST00000541159.5:c.1798T>C
|
ENSP00000438711.1:n.1798T>C
|
|
ENST00000542898.5:c.*532T>C
|
ENSP00000444615.1:n.*532T>C
|
|
ENST00000570511.5:c.1661T>C
|
ENSP00000458312.1:n.1661T>C
|
|
ENST00000572244.5:c.946T>C
|
ENSP00000461186.1:n.946T>C
|
|
ENST00000574583.5:c.1028T>C
|
ENSP00000460269.1:n.1028T>C
|
|
ENST00000576315.5:c.1061T>C
|
ENSP00000460551.1:n.1061T>C
|
|
ENST00000621655.1:c.1793T>C
|
ENSP00000481436.1:n.1793T>C
|
|
NM_000243.2:c.2256T>C , LRG_190t1:c.2256T>C
|
NP_000234.1:p.Leu752=
|
|
NM_001198536.1:c.*460T>C
|
NP_001185465.1:n.*460T>C
|
|
XM_017023236.2:c.2253T>C
|
XP_016878725.1:p.Leu751=
|
|
NM_000243.3:c.2256T>C
MANE Select
|
NP_000234.1:p.Leu752=
|
|
NM_001198536.2:c.*460T>C
|
NP_001185465.2:n.*460T>C
|
|