ENST00000697124.1:n.1293C>G
|
|
|
ENST00000219596.6:c.2172C>G
MANE Select
|
ENSP00000219596.1:p.Tyr724Ter
|
|
ENST00000219596.5:c.2172C>G
|
ENSP00000219596.1:p.Tyr724Ter
|
|
ENST00000339854.8:c.1632C>G
|
ENSP00000339639.4:p.Tyr544Ter
|
|
ENST00000536379.5:c.1539C>G
|
ENSP00000445079.1:p.Tyr513Ter
|
|
ENST00000536980.5:c.*448C>G
|
ENSP00000444178.1:n.*448C>G
|
|
ENST00000537682.5:c.*448C>G
|
ENSP00000438611.1:n.*448C>G
|
|
ENST00000538326.5:c.*797C>G
|
ENSP00000437486.1:n.*797C>G
|
|
ENST00000539145.5:c.1093C>G
|
ENSP00000444471.1:n.1093C>G
|
|
ENST00000541159.5:c.1714C>G
|
ENSP00000438711.1:n.1714C>G
|
|
ENST00000542898.5:c.*448C>G
|
ENSP00000444615.1:n.*448C>G
|
|
ENST00000570511.5:c.1577C>G
|
ENSP00000458312.1:n.1577C>G
|
|
ENST00000572244.5:c.862C>G
|
ENSP00000461186.1:n.862C>G
|
|
ENST00000574583.5:c.944C>G
|
ENSP00000460269.1:n.944C>G
|
|
ENST00000576315.5:c.977C>G
|
ENSP00000460551.1:n.977C>G
|
|
ENST00000621655.1:c.1709C>G
|
ENSP00000481436.1:n.1709C>G
|
|
NM_000243.2:c.2172C>G , LRG_190t1:c.2172C>G
|
NP_000234.1:p.Tyr724Ter
|
|
NM_001198536.1:c.*376C>G
|
NP_001185465.1:n.*376C>G
|
|
XM_017023236.2:c.2169C>G
|
XP_016878725.1:p.Tyr723Ter
|
|
NM_000243.3:c.2172C>G
MANE Select
|
NP_000234.1:p.Tyr724Ter
|
|
NM_001198536.2:c.*376C>G
|
NP_001185465.2:n.*376C>G
|
|