ENST00000409709.9:c.6101T>C
MANE Select
|
ENSP00000386331.3:p.Val2034Ala
|
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ENST00000670577.1:c.3902T>C
|
|
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ENST00000409619.6:c.5954T>C
|
ENSP00000386635.2:p.Val1985Ala
|
|
ENST00000409709.7:c.6101T>C
|
ENSP00000386331.3:p.Val2034Ala
|
|
ENST00000458169.2:c.3527T>C
|
ENSP00000417017.2:p.Val1176Ala
|
|
ENST00000458637.6:c.5987T>C
|
ENSP00000392185.2:p.Val1996Ala
|
|
ENST00000481328.7:n.3637T>C
|
|
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ENST00000526863.2:n.25+290T>C
|
|
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ENST00000605744.1:n.1568T>C
|
|
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NM_000260.3:c.6101T>C
|
NP_000251.3:p.Val2034Ala
|
|
NM_001127180.1:c.5987T>C
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NP_001120652.1:p.Val1996Ala
|
|
XM_005274012.2:c.5984T>C
|
XP_005274069.1:p.Val1995Ala
|
|
XM_006718558.2:c.6092T>C
|
XP_006718621.1:p.Val2031Ala
|
|
XM_006718559.2:c.5987T>C
|
XP_006718622.1:p.Val1996Ala
|
|
XM_006718560.2:c.5984T>C
|
XP_006718623.1:p.Val1995Ala
|
|
XM_006718561.2:c.5987T>C
|
XP_006718624.1:p.Val1996Ala
|
|
XM_011545044.1:c.6101T>C
|
XP_011543346.1:p.Val2034Ala
|
|
XM_011545045.1:c.6095T>C
|
XP_011543347.1:p.Val2032Ala
|
|
XM_011545046.1:c.6068T>C
|
XP_011543348.1:p.Val2023Ala
|
|
XM_011545047.1:c.6005T>C
|
XP_011543349.1:p.Val2002Ala
|
|
XM_011545048.1:c.5876T>C
|
XP_011543350.1:p.Val1959Ala
|
|
XM_011545049.1:c.5864T>C
|
XP_011543351.1:p.Val1955Ala
|
|
XM_011545050.1:c.5837T>C
|
XP_011543352.1:p.Val1946Ala
|
|
XM_011545051.1:c.6101T>C
|
XP_011543353.1:p.Val2034Ala
|
|
XR_949938.1:n.6421T>C
|
|
|
XR_949941.1:n.6395T>C
|
|
|
XM_011545044.2:c.6101T>C
|
XP_011543346.1:p.Val2034Ala
|
|
XM_011545046.2:c.6191T>C
|
XP_011543348.2:p.Val2064Ala
|
|
XM_011545050.2:c.5837T>C
|
XP_011543352.1:p.Val1946Ala
|
|
XM_017017778.1:c.6185T>C
|
XP_016873267.1:p.Val2062Ala
|
|
XM_017017779.1:c.6182T>C
|
XP_016873268.1:p.Val2061Ala
|
|
XM_017017780.1:c.6191T>C
|
XP_016873269.1:p.Val2064Ala
|
|
XM_017017781.1:c.6095T>C
|
XP_016873270.1:p.Val2032Ala
|
|
XM_017017782.1:c.6077T>C
|
XP_016873271.1:p.Val2026Ala
|
|
XM_017017783.1:c.6074T>C
|
XP_016873272.1:p.Val2025Ala
|
|
XM_017017784.1:c.6074T>C
|
XP_016873273.1:p.Val2025Ala
|
|
XM_017017785.1:c.5954T>C
|
XP_016873274.1:p.Val1985Ala
|
|
XM_017017786.1:c.6191T>C
|
XP_016873275.1:p.Val2064Ala
|
|
XM_017017788.1:c.6077T>C
|
XP_016873277.1:p.Val2026Ala
|
|
XR_001747885.1:n.6180T>C
|
|
|
XR_001747886.1:n.6121T>C
|
|
|
XR_001747887.1:n.6166T>C
|
|
|
NM_000260.4:c.6101T>C
MANE Select
|
NP_000251.3:p.Val2034Ala
|
|
NM_001127180.2:c.5987T>C
|
NP_001120652.1:p.Val1996Ala
|
|
NM_001369365.1:c.5954T>C
|
NP_001356294.1:p.Val1985Ala
|
|