ENST00000381365.4:c.*1750C>A
(C17orf107)
MANE Select
|
ENSP00000370770.3:n.*1750C>A
|
|
ENST00000649488.2:c.278G>T
(CHRNE)
MANE Select
|
ENSP00000497829.1:p.Gly93Val
|
|
ENST00000649830.1:c.-656G>T
(CHRNE)
|
ENSP00000496907.1:n.-656G>T
|
|
ENST00000293780.4:c.278G>T
(CHRNE)
|
ENSP00000293780.4:p.Gly93Val
|
|
ENST00000381365.3:c.*1750C>A
(C17orf107)
|
ENSP00000370770.3:n.*1750C>A
|
|
ENST00000575637.1:n.99G>T
(CHRNE)
|
|
|
NM_000080.3:c.278G>T
(CHRNE)
|
NP_000071.1:p.Gly93Val
|
|
NM_001145536.1:c.*1750C>A
(C17orf107)
|
NP_001139008.1:n.*1750C>A
|
|
XM_011523612.1:c.546+1777C>A
(C17orf107)
|
XP_011521914.1:n.546+1777C>A
|
|
XM_011523631.1:c.278G>T
(CHRNE)
|
XP_011521933.1:p.Gly93Val
|
|
NM_000080.4:c.278G>T
(CHRNE)
MANE Select
|
NP_000071.1:p.Gly93Val
|
|
XM_017024115.1:c.242G>T
(CHRNE)
|
XP_016879604.1:p.Gly81Val
|
|
XR_001752421.1:n.1123G>T
(CHRNE)
|
|
|
NM_001145536.2:c.*1750C>A
(C17orf107)
MANE Select
|
NP_001139008.1:n.*1750C>A
|
|