ENST00000460843.6:c.1923G>C
MANE Select
|
ENSP00000417980.1:p.Thr641=
|
|
ENST00000636027.1:c.1809G>C
|
ENSP00000489961.1:p.Thr603=
|
|
ENST00000637161.1:c.1830G>C
|
ENSP00000490328.1:p.Thr610=
|
|
ENST00000637261.1:c.1963G>C
|
ENSP00000490815.1:n.1963G>C
|
|
ENST00000638071.1:c.1550G>C
|
|
|
ENST00000640639.1:c.1092G>C
|
ENSP00000491823.1:p.Thr364=
|
|
ENST00000371394.6:c.*1658G>C
|
ENSP00000485945.1:n.*1658G>C
|
|
ENST00000460843.5:c.1923G>C
|
ENSP00000417980.1:p.Thr641=
|
|
ENST00000462484.5:c.1923G>C
|
ENSP00000417328.1:p.Thr641=
|
|
ENST00000462942.3:c.780G>C
|
ENSP00000436107.1:p.Thr260=
|
|
ENST00000465566.2:c.471G>C
|
ENSP00000486261.1:p.Thr157=
|
|
ENST00000626603.1:n.1700C>G
|
|
|
NM_001145527.1:c.1923G>C
|
NP_001138999.1:p.Thr641=
|
|
NM_024757.4:c.1923G>C
|
NP_079033.4:p.Thr641=
|
|
XM_005266105.3:c.1914G>C
|
XP_005266162.1:p.Thr638=
|
|
XM_005266110.1:c.1830G>C
|
XP_005266167.1:p.Thr610=
|
|
XM_006717288.2:c.1905G>C
|
XP_006717351.1:p.Thr635=
|
|
XM_011519021.1:c.1932G>C
|
XP_011517323.1:p.Thr644=
|
|
XM_011519022.1:c.1929G>C
|
XP_011517324.1:p.Thr643=
|
|
XM_011519023.1:c.1911G>C
|
XP_011517325.1:p.Thr637=
|
|
XM_011519024.1:c.1854G>C
|
XP_011517326.1:p.Thr618=
|
|
XM_011519025.1:c.1830G>C
|
XP_011517327.1:p.Thr610=
|
|
XM_011519026.1:c.1788G>C
|
XP_011517328.1:p.Thr596=
|
|
XM_011519027.1:c.1932G>C
|
XP_011517329.1:p.Thr644=
|
|
XM_011519028.1:c.1932G>C
|
XP_011517330.1:p.Thr644=
|
|
XM_011519029.1:c.354G>C
|
XP_011517331.1:p.Thr118=
|
|
XM_011519033.1:c.1767G>C
|
XP_011517335.1:p.Thr589=
|
|
NM_001354259.1:c.1830G>C
|
NP_001341188.1:p.Thr610=
|
|
NM_001354263.1:c.1902G>C
|
NP_001341192.1:p.Thr634=
|
|
XM_005266105.5:c.1914G>C
|
XP_005266162.1:p.Thr638=
|
|
XM_011519021.3:c.1932G>C
|
XP_011517323.1:p.Thr644=
|
|
XM_011519022.3:c.1929G>C
|
XP_011517324.1:p.Thr643=
|
|
XM_011519023.3:c.1911G>C
|
XP_011517325.1:p.Thr637=
|
|
XM_011519029.3:c.354G>C
|
XP_011517331.1:p.Thr118=
|
|
XM_017015134.1:c.1908G>C
|
XP_016870623.1:p.Thr636=
|
|
XM_017015136.2:c.1824G>C
|
XP_016870625.1:p.Thr608=
|
|
XM_017015137.1:c.1809G>C
|
XP_016870626.1:p.Thr603=
|
|
XM_017015138.1:c.1809G>C
|
XP_016870627.1:p.Thr603=
|
|
XM_024447674.1:c.1752G>C
|
XP_024303442.1:p.Thr584=
|
|
XM_024447675.1:c.1686G>C
|
XP_024303443.1:p.Thr562=
|
|
XM_024447676.1:c.1047G>C
|
XP_024303444.1:p.Thr349=
|
|
XM_024447677.1:c.1047G>C
|
XP_024303445.1:p.Thr349=
|
|
XM_024447678.1:c.1830G>C
|
XP_024303446.1:p.Thr610=
|
|
XM_024447679.1:c.1830G>C
|
XP_024303447.1:p.Thr610=
|
|
XM_024447680.1:c.1665G>C
|
XP_024303448.1:p.Thr555=
|
|
NM_024757.5:c.1923G>C
MANE Select
|
NP_079033.4:p.Thr641=
|
|
NM_001145527.2:c.1923G>C
|
NP_001138999.1:p.Thr641=
|
|
NM_001354259.2:c.1830G>C
|
NP_001341188.1:p.Thr610=
|
|
NM_001354263.2:c.1902G>C
|
NP_001341192.1:p.Thr634=
|
|