|
NM_017802.4:c.2425A>G
MANE Select
|
NP_060272.3:p.Ile809Val
|
|
ENST00000297440.11:c.2425A>G
MANE Select
|
ENSP00000297440.6:p.Ile809Val
|
|
NM_017802.3:c.2425A>G
|
NP_060272.3:p.Ile809Val
|
|
NR_075098.1:n.2383A>G
|
|
|
NR_075098.2:n.2385A>G
|
|
|
ENST00000297440.10:c.2425A>G
|
ENSP00000297440.6:p.Ile809Val
|
|
ENST00000403952.3:c.700A>G
|
ENSP00000384884.3:p.Ile234Val
|
|
ENST00000440747.5:c.1829A>G
|
|
|
ENST00000461576.1:n.235A>G
|
|
|
XM_024446813.1:c.2239+4976A>G
|
XP_024302581.1:n.2239+4976A>G
|
|
XM_024446814.1:c.1819A>G
|
XP_024302582.1:p.Ile607Val
|