|
ENST00000269217.11:c.4719T>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Leu1573=
|
|
|
ENST00000313654.14:c.9546T>G
MANE Select
|
ENSP00000324532.8:p.Leu3182=
|
|
|
ENST00000649721.1:c.6141T>G
|
ENSP00000497885.1:p.Leu2047=
|
|
|
ENST00000269217.10:c.4719T>G
|
ENSP00000269217.5:p.Leu1573=
|
|
|
ENST00000313654.13:c.9546T>G
|
ENSP00000324532.8:p.Leu3182=
|
|
|
ENST00000399516.7:c.9378T>G
|
ENSP00000382432.2:p.Leu3126=
|
|
|
ENST00000587184.5:c.4551T>G
|
ENSP00000466557.1:p.Leu1517=
|
|
|
ENST00000588004.1:c.67T>G
|
|
|
|
ENST00000588770.5:n.4124T>G
|
|
|
|
NM_000227.4:c.4719T>G
|
NP_000218.3:p.Leu1573=
|
|
|
NM_001127717.2:c.9378T>G
|
NP_001121189.2:p.Leu3126=
|
|
|
NM_001127718.2:c.4551T>G
|
NP_001121190.2:p.Leu1517=
|
|
|
NM_198129.2:c.9546T>G
|
NP_937762.2:p.Leu3182=
|
|
|
XM_011525978.1:c.9573T>G
|
XP_011524280.1:p.Leu3191=
|
|
|
XM_011525979.1:c.9564T>G
|
XP_011524281.1:p.Leu3188=
|
|
|
XM_011525980.1:c.9555T>G
|
XP_011524282.1:p.Leu3185=
|
|
|
XM_011525981.1:c.9441T>G
|
XP_011524283.1:p.Leu3147=
|
|
|
XM_011525982.1:c.9276T>G
|
XP_011524284.1:p.Leu3092=
|
|
|
XM_011525978.2:c.9573T>G
|
XP_011524280.1:p.Leu3191=
|
|
|
XM_011525979.2:c.9564T>G
|
XP_011524281.1:p.Leu3188=
|
|
|
XM_011525980.2:c.9555T>G
|
XP_011524282.1:p.Leu3185=
|
|
|
XM_011525981.2:c.9441T>G
|
XP_011524283.1:p.Leu3147=
|
|
|
XM_011525982.2:c.9276T>G
|
XP_011524284.1:p.Leu3092=
|
|
|
XM_017025743.1:c.7425T>G
|
XP_016881232.1:p.Leu2475=
|
|
|
XM_017025744.1:c.5115T>G
|
XP_016881233.1:p.Leu1705=
|
|
|
XR_001753199.1:n.9814T>G
|
|
|
|
NM_000227.5:c.4719T>G
|
NP_000218.3:p.Leu1573=
|
|
|
NM_001127717.3:c.9378T>G
|
NP_001121189.2:p.Leu3126=
|
|
|
NM_001127718.3:c.4551T>G
|
NP_001121190.2:p.Leu1517=
|
|
|
NM_198129.3:c.9546T>G
|
NP_937762.2:p.Leu3182=
|
|
|
NM_000227.6:c.4719T>G
MANE Plus Clinical
|
NP_000218.3:p.Leu1573=
|
|
|
NM_001127717.4:c.9378T>G
|
NP_001121189.2:p.Leu3126=
|
|
|
NM_001127718.4:c.4551T>G
|
NP_001121190.2:p.Leu1517=
|
|
|
NM_198129.4:c.9546T>G
MANE Select
|
NP_937762.2:p.Leu3182=
|
|
