|
ENST00000269217.11:c.4722T>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Val1574=
|
|
|
ENST00000313654.14:c.9549T>G
MANE Select
|
ENSP00000324532.8:p.Val3183=
|
|
|
ENST00000649721.1:c.6144T>G
|
ENSP00000497885.1:p.Val2048=
|
|
|
ENST00000269217.10:c.4722T>G
|
ENSP00000269217.5:p.Val1574=
|
|
|
ENST00000313654.13:c.9549T>G
|
ENSP00000324532.8:p.Val3183=
|
|
|
ENST00000399516.7:c.9381T>G
|
ENSP00000382432.2:p.Val3127=
|
|
|
ENST00000587184.5:c.4554T>G
|
ENSP00000466557.1:p.Val1518=
|
|
|
ENST00000588004.1:c.70T>G
|
|
|
|
ENST00000588770.5:n.4127T>G
|
|
|
|
NM_000227.4:c.4722T>G
|
NP_000218.3:p.Val1574=
|
|
|
NM_001127717.2:c.9381T>G
|
NP_001121189.2:p.Val3127=
|
|
|
NM_001127718.2:c.4554T>G
|
NP_001121190.2:p.Val1518=
|
|
|
NM_198129.2:c.9549T>G
|
NP_937762.2:p.Val3183=
|
|
|
XM_011525978.1:c.9576T>G
|
XP_011524280.1:p.Val3192=
|
|
|
XM_011525979.1:c.9567T>G
|
XP_011524281.1:p.Val3189=
|
|
|
XM_011525980.1:c.9558T>G
|
XP_011524282.1:p.Val3186=
|
|
|
XM_011525981.1:c.9444T>G
|
XP_011524283.1:p.Val3148=
|
|
|
XM_011525982.1:c.9279T>G
|
XP_011524284.1:p.Val3093=
|
|
|
XM_011525978.2:c.9576T>G
|
XP_011524280.1:p.Val3192=
|
|
|
XM_011525979.2:c.9567T>G
|
XP_011524281.1:p.Val3189=
|
|
|
XM_011525980.2:c.9558T>G
|
XP_011524282.1:p.Val3186=
|
|
|
XM_011525981.2:c.9444T>G
|
XP_011524283.1:p.Val3148=
|
|
|
XM_011525982.2:c.9279T>G
|
XP_011524284.1:p.Val3093=
|
|
|
XM_017025743.1:c.7428T>G
|
XP_016881232.1:p.Val2476=
|
|
|
XM_017025744.1:c.5118T>G
|
XP_016881233.1:p.Val1706=
|
|
|
XR_001753199.1:n.9817T>G
|
|
|
|
NM_000227.5:c.4722T>G
|
NP_000218.3:p.Val1574=
|
|
|
NM_001127717.3:c.9381T>G
|
NP_001121189.2:p.Val3127=
|
|
|
NM_001127718.3:c.4554T>G
|
NP_001121190.2:p.Val1518=
|
|
|
NM_198129.3:c.9549T>G
|
NP_937762.2:p.Val3183=
|
|
|
NM_000227.6:c.4722T>G
MANE Plus Clinical
|
NP_000218.3:p.Val1574=
|
|
|
NM_001127717.4:c.9381T>G
|
NP_001121189.2:p.Val3127=
|
|
|
NM_001127718.4:c.4554T>G
|
NP_001121190.2:p.Val1518=
|
|
|
NM_198129.4:c.9549T>G
MANE Select
|
NP_937762.2:p.Val3183=
|
|
