ENST00000269217.11:c.926C>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Thr309Arg
|
|
ENST00000313654.14:c.5753C>G
MANE Select
|
ENSP00000324532.8:p.Thr1918Arg
|
|
ENST00000649721.1:c.2645C>G
|
ENSP00000497885.1:p.Thr882Arg
|
|
ENST00000269217.10:c.926C>G
|
ENSP00000269217.5:p.Thr309Arg
|
|
ENST00000313654.13:c.5753C>G
|
ENSP00000324532.8:p.Thr1918Arg
|
|
ENST00000399516.7:c.5753C>G
|
ENSP00000382432.2:p.Thr1918Arg
|
|
ENST00000586709.1:n.141C>G
|
|
|
ENST00000586751.5:c.531C>G
|
|
|
ENST00000587184.5:c.926C>G
|
ENSP00000466557.1:p.Thr309Arg
|
|
ENST00000588770.5:n.331C>G
|
|
|
NM_000227.4:c.926C>G
|
NP_000218.3:p.Thr309Arg
|
|
NM_001127717.2:c.5753C>G
|
NP_001121189.2:p.Thr1918Arg
|
|
NM_001127718.2:c.926C>G
|
NP_001121190.2:p.Thr309Arg
|
|
NM_198129.2:c.5753C>G
|
NP_937762.2:p.Thr1918Arg
|
|
XM_011525978.1:c.5780C>G
|
XP_011524280.1:p.Thr1927Arg
|
|
XM_011525979.1:c.5771C>G
|
XP_011524281.1:p.Thr1924Arg
|
|
XM_011525980.1:c.5762C>G
|
XP_011524282.1:p.Thr1921Arg
|
|
XM_011525981.1:c.5648C>G
|
XP_011524283.1:p.Thr1883Arg
|
|
XM_011525982.1:c.5780C>G
|
XP_011524284.1:p.Thr1927Arg
|
|
XM_011525978.2:c.5780C>G
|
XP_011524280.1:p.Thr1927Arg
|
|
XM_011525979.2:c.5771C>G
|
XP_011524281.1:p.Thr1924Arg
|
|
XM_011525980.2:c.5762C>G
|
XP_011524282.1:p.Thr1921Arg
|
|
XM_011525981.2:c.5648C>G
|
XP_011524283.1:p.Thr1883Arg
|
|
XM_011525982.2:c.5780C>G
|
XP_011524284.1:p.Thr1927Arg
|
|
XM_017025743.1:c.3632C>G
|
XP_016881232.1:p.Thr1211Arg
|
|
XM_017025744.1:c.1322C>G
|
XP_016881233.1:p.Thr441Arg
|
|
XR_001753199.1:n.6021C>G
|
|
|
NM_000227.5:c.926C>G
|
NP_000218.3:p.Thr309Arg
|
|
NM_001127717.3:c.5753C>G
|
NP_001121189.2:p.Thr1918Arg
|
|
NM_001127718.3:c.926C>G
|
NP_001121190.2:p.Thr309Arg
|
|
NM_198129.3:c.5753C>G
|
NP_937762.2:p.Thr1918Arg
|
|
NM_000227.6:c.926C>G
MANE Plus Clinical
|
NP_000218.3:p.Thr309Arg
|
|
NM_001127717.4:c.5753C>G
|
NP_001121189.2:p.Thr1918Arg
|
|
NM_001127718.4:c.926C>G
|
NP_001121190.2:p.Thr309Arg
|
|
NM_198129.4:c.5753C>G
MANE Select
|
NP_937762.2:p.Thr1918Arg
|
|