|
ENST00000269217.11:c.4668A>T
MANE Plus Clinical
|
ENSP00000269217.5:p.Gly1556=
|
|
|
ENST00000313654.14:c.9495A>T
MANE Select
|
ENSP00000324532.8:p.Gly3165=
|
|
|
ENST00000649721.1:c.6090A>T
|
ENSP00000497885.1:p.Gly2030=
|
|
|
ENST00000269217.10:c.4668A>T
|
ENSP00000269217.5:p.Gly1556=
|
|
|
ENST00000313654.13:c.9495A>T
|
ENSP00000324532.8:p.Gly3165=
|
|
|
ENST00000399516.7:c.9327A>T
|
ENSP00000382432.2:p.Gly3109=
|
|
|
ENST00000587184.5:c.4500A>T
|
ENSP00000466557.1:p.Gly1500=
|
|
|
ENST00000588004.1:c.16A>T
|
|
|
|
ENST00000588770.5:n.4073A>T
|
|
|
|
NM_000227.4:c.4668A>T
|
NP_000218.3:p.Gly1556=
|
|
|
NM_001127717.2:c.9327A>T
|
NP_001121189.2:p.Gly3109=
|
|
|
NM_001127718.2:c.4500A>T
|
NP_001121190.2:p.Gly1500=
|
|
|
NM_198129.2:c.9495A>T
|
NP_937762.2:p.Gly3165=
|
|
|
XM_011525978.1:c.9522A>T
|
XP_011524280.1:p.Gly3174=
|
|
|
XM_011525979.1:c.9513A>T
|
XP_011524281.1:p.Gly3171=
|
|
|
XM_011525980.1:c.9504A>T
|
XP_011524282.1:p.Gly3168=
|
|
|
XM_011525981.1:c.9390A>T
|
XP_011524283.1:p.Gly3130=
|
|
|
XM_011525982.1:c.9225A>T
|
XP_011524284.1:p.Gly3075=
|
|
|
XM_011525978.2:c.9522A>T
|
XP_011524280.1:p.Gly3174=
|
|
|
XM_011525979.2:c.9513A>T
|
XP_011524281.1:p.Gly3171=
|
|
|
XM_011525980.2:c.9504A>T
|
XP_011524282.1:p.Gly3168=
|
|
|
XM_011525981.2:c.9390A>T
|
XP_011524283.1:p.Gly3130=
|
|
|
XM_011525982.2:c.9225A>T
|
XP_011524284.1:p.Gly3075=
|
|
|
XM_017025743.1:c.7374A>T
|
XP_016881232.1:p.Gly2458=
|
|
|
XM_017025744.1:c.5064A>T
|
XP_016881233.1:p.Gly1688=
|
|
|
XR_001753199.1:n.9763A>T
|
|
|
|
NM_000227.5:c.4668A>T
|
NP_000218.3:p.Gly1556=
|
|
|
NM_001127717.3:c.9327A>T
|
NP_001121189.2:p.Gly3109=
|
|
|
NM_001127718.3:c.4500A>T
|
NP_001121190.2:p.Gly1500=
|
|
|
NM_198129.3:c.9495A>T
|
NP_937762.2:p.Gly3165=
|
|
|
NM_000227.6:c.4668A>T
MANE Plus Clinical
|
NP_000218.3:p.Gly1556=
|
|
|
NM_001127717.4:c.9327A>T
|
NP_001121189.2:p.Gly3109=
|
|
|
NM_001127718.4:c.4500A>T
|
NP_001121190.2:p.Gly1500=
|
|
|
NM_198129.4:c.9495A>T
MANE Select
|
NP_937762.2:p.Gly3165=
|
|
