|
ENST00000269217.11:c.4650T>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Ile1550Met
|
|
|
ENST00000313654.14:c.9477T>G
MANE Select
|
ENSP00000324532.8:p.Ile3159Met
|
|
|
ENST00000649721.1:c.6072T>G
|
ENSP00000497885.1:p.Ile2024Met
|
|
|
ENST00000269217.10:c.4650T>G
|
ENSP00000269217.5:p.Ile1550Met
|
|
|
ENST00000313654.13:c.9477T>G
|
ENSP00000324532.8:p.Ile3159Met
|
|
|
ENST00000399516.7:c.9309T>G
|
ENSP00000382432.2:p.Ile3103Met
|
|
|
ENST00000587184.5:c.4482T>G
|
ENSP00000466557.1:p.Ile1494Met
|
|
|
ENST00000588770.5:n.4055T>G
|
|
|
|
NM_000227.4:c.4650T>G
|
NP_000218.3:p.Ile1550Met
|
|
|
NM_001127717.2:c.9309T>G
|
NP_001121189.2:p.Ile3103Met
|
|
|
NM_001127718.2:c.4482T>G
|
NP_001121190.2:p.Ile1494Met
|
|
|
NM_198129.2:c.9477T>G
|
NP_937762.2:p.Ile3159Met
|
|
|
XM_011525978.1:c.9504T>G
|
XP_011524280.1:p.Ile3168Met
|
|
|
XM_011525979.1:c.9495T>G
|
XP_011524281.1:p.Ile3165Met
|
|
|
XM_011525980.1:c.9486T>G
|
XP_011524282.1:p.Ile3162Met
|
|
|
XM_011525981.1:c.9372T>G
|
XP_011524283.1:p.Ile3124Met
|
|
|
XM_011525982.1:c.9207T>G
|
XP_011524284.1:p.Ile3069Met
|
|
|
XM_011525978.2:c.9504T>G
|
XP_011524280.1:p.Ile3168Met
|
|
|
XM_011525979.2:c.9495T>G
|
XP_011524281.1:p.Ile3165Met
|
|
|
XM_011525980.2:c.9486T>G
|
XP_011524282.1:p.Ile3162Met
|
|
|
XM_011525981.2:c.9372T>G
|
XP_011524283.1:p.Ile3124Met
|
|
|
XM_011525982.2:c.9207T>G
|
XP_011524284.1:p.Ile3069Met
|
|
|
XM_017025743.1:c.7356T>G
|
XP_016881232.1:p.Ile2452Met
|
|
|
XM_017025744.1:c.5046T>G
|
XP_016881233.1:p.Ile1682Met
|
|
|
XR_001753199.1:n.9745T>G
|
|
|
|
NM_000227.5:c.4650T>G
|
NP_000218.3:p.Ile1550Met
|
|
|
NM_001127717.3:c.9309T>G
|
NP_001121189.2:p.Ile3103Met
|
|
|
NM_001127718.3:c.4482T>G
|
NP_001121190.2:p.Ile1494Met
|
|
|
NM_198129.3:c.9477T>G
|
NP_937762.2:p.Ile3159Met
|
|
|
NM_000227.6:c.4650T>G
MANE Plus Clinical
|
NP_000218.3:p.Ile1550Met
|
|
|
NM_001127717.4:c.9309T>G
|
NP_001121189.2:p.Ile3103Met
|
|
|
NM_001127718.4:c.4482T>G
|
NP_001121190.2:p.Ile1494Met
|
|
|
NM_198129.4:c.9477T>G
MANE Select
|
NP_937762.2:p.Ile3159Met
|
|
