ENST00000236147.6:c.577T>G
(SELL)
MANE Select
|
ENSP00000236147.5:p.Phe193Val
|
|
ENST00000650983.1:c.616T>G
(SELL)
|
ENSP00000498227.1:p.Phe206Val
|
|
ENST00000236147.4:c.616T>G
(SELL)
|
ENSP00000236147.4:p.Phe206Val
|
|
ENST00000463108.5:n.777T>G
(SELL)
|
|
|
ENST00000466340.1:n.589T>G
(SELL)
|
|
|
ENST00000479657.5:n.329T>G
(SELL)
|
|
|
ENST00000498289.5:n.851+23413A>C
(FIRRM)
|
|
|
NM_000655.4:c.616T>G
(SELL)
|
NP_000646.2:p.Phe206Val
|
|
NR_029467.1:n.545T>G
(SELL)
|
|
|
NM_000655.5:c.577T>G
(SELL)
MANE Select
|
NP_000646.3:p.Phe193Val
|
|
NR_029467.2:n.546T>G
(SELL)
|
|
|