|
NM_015346.4:c.1944T>C
MANE Select
|
NP_056161.2:p.His648=
|
|
ENST00000347230.9:c.1944T>C
MANE Select
|
ENSP00000251119.5:p.His648=
|
|
NM_015346.3:c.1944T>C
|
NP_056161.2:p.His648=
|
|
ENST00000347230.8:c.1944T>C
|
ENSP00000251119.5:p.His648=
|
|
ENST00000554523.5:n.2081T>C
|
|
|
ENST00000554557.5:c.*241T>C
|
ENSP00000450431.1:n.*241T>C
|
|
ENST00000555452.1:c.1944T>C
|
ENSP00000450603.1:p.His648=
|
|
ENST00000557366.5:n.1990T>C
|
|
|
ENST00000557407.1:n.2079T>C
|
|
|
ENST00000676512.1:c.1944T>C
|
ENSP00000504552.1:p.His648=
|
|
ENST00000676620.1:c.1944T>C
|
ENSP00000504587.1:p.His648=
|
|
ENST00000677026.1:c.1740T>C
|
ENSP00000503710.1:p.His580=
|
|
ENST00000678382.1:c.*939T>C
|
ENSP00000504130.1:n.*939T>C
|
|
ENST00000678386.1:c.1944T>C
|
ENSP00000503677.1:p.His648=
|
|
XM_006720093.2:c.1944T>C
|
XP_006720156.1:p.His648=
|
|
XM_011536606.1:c.435T>C
|
XP_011534908.1:p.His145=
|
|
XM_011536609.1:c.1944T>C
|
XP_011534911.1:p.His648=
|
|
XM_011536609.2:c.1944T>C
|
XP_011534911.1:p.His648=
|
|
XM_017021124.1:c.1944T>C
|
XP_016876613.1:p.His648=
|
|
XM_017021125.1:c.1944T>C
|
XP_016876614.1:p.His648=
|
|
XM_017021126.1:c.435T>C
|
XP_016876615.1:p.His145=
|