ENST00000262304.9:c.2033C>T
MANE Select
|
ENSP00000262304.4:p.Ala678Val
|
|
ENST00000262304.8:c.2033C>T
|
ENSP00000262304.4:p.Ala678Val
|
|
ENST00000423118.5:c.2033C>T
|
ENSP00000399501.1:p.Ala678Val
|
|
ENST00000488185.2:c.472+2047C>T
|
|
|
ENST00000568591.5:c.964C>T
|
ENSP00000457162.1:n.964C>T
|
|
NM_000296.3:c.2033C>T
|
NP_000287.3:p.Ala678Val
|
|
NM_001009944.2:c.2033C>T
|
NP_001009944.2:p.Ala678Val
|
|
XM_011522525.1:c.2087C>T
|
XP_011520827.1:p.Ala696Val
|
|
XM_011522526.1:c.2087C>T
|
XP_011520828.1:p.Ala696Val
|
|
XM_011522527.1:c.2087C>T
|
XP_011520829.1:p.Ala696Val
|
|
XM_011522528.1:c.2087C>T
|
XP_011520830.1:p.Ala696Val
|
|
XM_011522529.1:c.2087C>T
|
XP_011520831.1:p.Ala696Val
|
|
XM_011522530.1:c.2033C>T
|
XP_011520832.1:p.Ala678Val
|
|
XM_011522531.1:c.2015C>T
|
XP_011520833.1:p.Ala672Val
|
|
XM_011522532.1:c.1961C>T
|
XP_011520834.1:p.Ala654Val
|
|
XM_011522533.1:c.1880C>T
|
XP_011520835.1:p.Ala627Val
|
|
XM_011522534.1:c.1823C>T
|
XP_011520836.1:p.Ala608Val
|
|
XM_011522536.1:c.2087C>T
|
XP_011520838.1:p.Ala696Val
|
|
XR_932867.1:n.2102C>T
|
|
|
XR_932868.1:n.2102C>T
|
|
|
XR_932869.1:n.2102C>T
|
|
|
XR_932870.1:n.2102C>T
|
|
|
XM_011522528.3:c.2087C>T
|
XP_011520830.1:p.Ala696Val
|
|
XM_011522529.2:c.2087C>T
|
XP_011520831.1:p.Ala696Val
|
|
XM_024450298.1:c.2033C>T
|
XP_024306066.1:p.Ala678Val
|
|
XM_024450299.1:c.1961C>T
|
XP_024306067.1:p.Ala654Val
|
|
XM_024450300.1:c.1823C>T
|
XP_024306068.1:p.Ala608Val
|
|
NM_000296.4:c.2033C>T
|
NP_000287.4:p.Ala678Val
|
|
NM_001009944.3:c.2033C>T
MANE Select
|
NP_001009944.3:p.Ala678Val
|
|