ENST00000269217.11:c.186A>T
MANE Plus Clinical
|
ENSP00000269217.5:p.Gly62=
|
|
ENST00000313654.14:c.5013A>T
MANE Select
|
ENSP00000324532.8:p.Gly1671=
|
|
ENST00000649721.1:c.1905A>T
|
ENSP00000497885.1:p.Gly635=
|
|
ENST00000269217.10:c.186A>T
|
ENSP00000269217.5:p.Gly62=
|
|
ENST00000313654.13:c.5013A>T
|
ENSP00000324532.8:p.Gly1671=
|
|
ENST00000399516.7:c.5013A>T
|
ENSP00000382432.2:p.Gly1671=
|
|
ENST00000587184.5:c.186A>T
|
ENSP00000466557.1:p.Gly62=
|
|
NM_000227.4:c.186A>T
|
NP_000218.3:p.Gly62=
|
|
NM_001127717.2:c.5013A>T
|
NP_001121189.2:p.Gly1671=
|
|
NM_001127718.2:c.186A>T
|
NP_001121190.2:p.Gly62=
|
|
NM_198129.2:c.5013A>T
|
NP_937762.2:p.Gly1671=
|
|
XM_011525978.1:c.5040A>T
|
XP_011524280.1:p.Gly1680=
|
|
XM_011525979.1:c.5031A>T
|
XP_011524281.1:p.Gly1677=
|
|
XM_011525980.1:c.5022A>T
|
XP_011524282.1:p.Gly1674=
|
|
XM_011525981.1:c.4908A>T
|
XP_011524283.1:p.Gly1636=
|
|
XM_011525982.1:c.5040A>T
|
XP_011524284.1:p.Gly1680=
|
|
XM_011525978.2:c.5040A>T
|
XP_011524280.1:p.Gly1680=
|
|
XM_011525979.2:c.5031A>T
|
XP_011524281.1:p.Gly1677=
|
|
XM_011525980.2:c.5022A>T
|
XP_011524282.1:p.Gly1674=
|
|
XM_011525981.2:c.4908A>T
|
XP_011524283.1:p.Gly1636=
|
|
XM_011525982.2:c.5040A>T
|
XP_011524284.1:p.Gly1680=
|
|
XM_017025743.1:c.2892A>T
|
XP_016881232.1:p.Gly964=
|
|
XM_017025744.1:c.582A>T
|
XP_016881233.1:p.Gly194=
|
|
XR_001753199.1:n.5281A>T
|
|
|
NM_000227.5:c.186A>T
|
NP_000218.3:p.Gly62=
|
|
NM_001127717.3:c.5013A>T
|
NP_001121189.2:p.Gly1671=
|
|
NM_001127718.3:c.186A>T
|
NP_001121190.2:p.Gly62=
|
|
NM_198129.3:c.5013A>T
|
NP_937762.2:p.Gly1671=
|
|
NM_000227.6:c.186A>T
MANE Plus Clinical
|
NP_000218.3:p.Gly62=
|
|
NM_001127717.4:c.5013A>T
|
NP_001121189.2:p.Gly1671=
|
|
NM_001127718.4:c.186A>T
|
NP_001121190.2:p.Gly62=
|
|
NM_198129.4:c.5013A>T
MANE Select
|
NP_937762.2:p.Gly1671=
|
|