|
ENST00000269217.11:c.1863C>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Ala621=
|
|
|
ENST00000313654.14:c.6690C>G
MANE Select
|
ENSP00000324532.8:p.Ala2230=
|
|
|
ENST00000649721.1:c.3582C>G
|
ENSP00000497885.1:p.Ala1194=
|
|
|
ENST00000269217.10:c.1863C>G
|
ENSP00000269217.5:p.Ala621=
|
|
|
ENST00000313654.13:c.6690C>G
|
ENSP00000324532.8:p.Ala2230=
|
|
|
ENST00000399516.7:c.6522C>G
|
ENSP00000382432.2:p.Ala2174=
|
|
|
ENST00000586751.5:c.1468C>G
|
|
|
|
ENST00000587184.5:c.1695C>G
|
ENSP00000466557.1:p.Ala565=
|
|
|
ENST00000588770.5:n.1268C>G
|
|
|
|
NM_000227.4:c.1863C>G
|
NP_000218.3:p.Ala621=
|
|
|
NM_001127717.2:c.6522C>G
|
NP_001121189.2:p.Ala2174=
|
|
|
NM_001127718.2:c.1695C>G
|
NP_001121190.2:p.Ala565=
|
|
|
NM_198129.2:c.6690C>G
|
NP_937762.2:p.Ala2230=
|
|
|
XM_011525978.1:c.6717C>G
|
XP_011524280.1:p.Ala2239=
|
|
|
XM_011525979.1:c.6708C>G
|
XP_011524281.1:p.Ala2236=
|
|
|
XM_011525980.1:c.6699C>G
|
XP_011524282.1:p.Ala2233=
|
|
|
XM_011525981.1:c.6585C>G
|
XP_011524283.1:p.Ala2195=
|
|
|
XM_011525982.1:c.6717C>G
|
XP_011524284.1:p.Ala2239=
|
|
|
XM_011525978.2:c.6717C>G
|
XP_011524280.1:p.Ala2239=
|
|
|
XM_011525979.2:c.6708C>G
|
XP_011524281.1:p.Ala2236=
|
|
|
XM_011525980.2:c.6699C>G
|
XP_011524282.1:p.Ala2233=
|
|
|
XM_011525981.2:c.6585C>G
|
XP_011524283.1:p.Ala2195=
|
|
|
XM_011525982.2:c.6717C>G
|
XP_011524284.1:p.Ala2239=
|
|
|
XM_017025743.1:c.4569C>G
|
XP_016881232.1:p.Ala1523=
|
|
|
XM_017025744.1:c.2259C>G
|
XP_016881233.1:p.Ala753=
|
|
|
XR_001753199.1:n.6958C>G
|
|
|
|
NM_000227.5:c.1863C>G
|
NP_000218.3:p.Ala621=
|
|
|
NM_001127717.3:c.6522C>G
|
NP_001121189.2:p.Ala2174=
|
|
|
NM_001127718.3:c.1695C>G
|
NP_001121190.2:p.Ala565=
|
|
|
NM_198129.3:c.6690C>G
|
NP_937762.2:p.Ala2230=
|
|
|
NM_000227.6:c.1863C>G
MANE Plus Clinical
|
NP_000218.3:p.Ala621=
|
|
|
NM_001127717.4:c.6522C>G
|
NP_001121189.2:p.Ala2174=
|
|
|
NM_001127718.4:c.1695C>G
|
NP_001121190.2:p.Ala565=
|
|
|
NM_198129.4:c.6690C>G
MANE Select
|
NP_937762.2:p.Ala2230=
|
|
