ENST00000697124.1:n.1408G>T
|
|
|
ENST00000219596.6:c.2287G>T
MANE Select
|
ENSP00000219596.1:p.Gly763Ter
|
|
ENST00000219596.5:c.2287G>T
|
ENSP00000219596.1:p.Gly763Ter
|
|
ENST00000339854.8:c.1747G>T
|
ENSP00000339639.4:p.Gly583Ter
|
|
ENST00000536379.5:c.1654G>T
|
ENSP00000445079.1:p.Gly552Ter
|
|
ENST00000536980.5:c.*563G>T
|
ENSP00000444178.1:n.*563G>T
|
|
ENST00000537682.5:c.*563G>T
|
ENSP00000438611.1:n.*563G>T
|
|
ENST00000538326.5:c.*912G>T
|
ENSP00000437486.1:n.*912G>T
|
|
ENST00000539145.5:c.1208G>T
|
ENSP00000444471.1:n.1208G>T
|
|
ENST00000541159.5:c.1829G>T
|
ENSP00000438711.1:n.1829G>T
|
|
ENST00000542898.5:c.*563G>T
|
ENSP00000444615.1:n.*563G>T
|
|
ENST00000570511.5:c.1692G>T
|
ENSP00000458312.1:n.1692G>T
|
|
ENST00000572244.5:c.977G>T
|
ENSP00000461186.1:n.977G>T
|
|
ENST00000574583.5:c.1059G>T
|
ENSP00000460269.1:n.1059G>T
|
|
ENST00000576315.5:c.1092G>T
|
ENSP00000460551.1:n.1092G>T
|
|
ENST00000621655.1:c.1824G>T
|
ENSP00000481436.1:n.1824G>T
|
|
NM_000243.2:c.2287G>T , LRG_190t1:c.2287G>T
|
NP_000234.1:p.Gly763Ter
|
|
NM_001198536.1:c.*491G>T
|
NP_001185465.1:n.*491G>T
|
|
XM_017023236.2:c.2284G>T
|
XP_016878725.1:p.Gly762Ter
|
|
NM_000243.3:c.2287G>T
MANE Select
|
NP_000234.1:p.Gly763Ter
|
|
NM_001198536.2:c.*491G>T
|
NP_001185465.2:n.*491G>T
|
|