ENST00000282516.13:c.3296C>T
MANE Select
|
ENSP00000282516.8:p.Ala1099Val
|
|
ENST00000652901.1:c.3296C>T
|
ENSP00000499536.1:p.Ala1099Val
|
|
ENST00000282516.12:c.3296C>T
|
ENSP00000282516.8:p.Ala1099Val
|
|
ENST00000448238.2:c.3296C>T
|
ENSP00000406266.2:p.Ala1099Val
|
|
ENST00000503274.1:n.647C>T
|
|
|
ENST00000504430.5:n.2916C>T
|
|
|
ENST00000509429.1:n.47C>T
|
|
|
ENST00000621733.1:c.1-68782C>T
|
ENSP00000480694.1:n.1-68782C>T
|
|
NM_015384.4:c.3296C>T
|
NP_056199.2:p.Ala1099Val
|
|
NM_133433.3:c.3296C>T
|
NP_597677.2:p.Ala1099Val
|
|
XM_005248280.2:c.3296C>T
|
XP_005248337.1:p.Ala1099Val
|
|
XM_005248282.3:c.2552C>T
|
XP_005248339.2:p.Ala851Val
|
|
XM_006714467.2:c.3296C>T
|
XP_006714530.1:p.Ala1099Val
|
|
XM_006714468.1:c.3296C>T
|
XP_006714531.1:p.Ala1099Val
|
|
XM_011514014.1:c.3122-5021C>T
|
XP_011512316.1:n.3122-5021C>T
|
|
XM_011514015.1:c.3296C>T
|
XP_011512317.1:p.Ala1099Val
|
|
XM_005248280.3:c.3296C>T
|
XP_005248337.1:p.Ala1099Val
|
|
XM_005248282.5:c.2636C>T
|
XP_005248339.3:p.Ala879Val
|
|
XM_006714468.2:c.3296C>T
|
XP_006714531.1:p.Ala1099Val
|
|
XM_017009329.1:c.3296C>T
|
XP_016864818.1:p.Ala1099Val
|
|
XM_017009330.2:c.1679C>T
|
XP_016864819.1:p.Ala560Val
|
|
XM_017009331.1:c.1670C>T
|
XP_016864820.1:p.Ala557Val
|
|
NM_133433.4:c.3296C>T
MANE Select
|
NP_597677.2:p.Ala1099Val
|
|
NM_015384.5:c.3296C>T
|
NP_056199.2:p.Ala1099Val
|
|