ENST00000360614.8:c.1977G>A
MANE Select
|
ENSP00000353826.2:p.Ser659=
|
|
ENST00000360614.7:c.1977G>A
|
ENSP00000353826.2:p.Ser659=
|
|
ENST00000540670.6:c.1389G>A
|
ENSP00000441523.1:p.Ser463=
|
|
ENST00000585374.5:c.1635G>A
|
ENSP00000465585.1:p.Ser545=
|
|
ENST00000587552.5:n.1715G>A
|
|
|
ENST00000590558.5:c.1784G>A
|
ENSP00000467808.1:n.1784G>A
|
|
ENST00000590729.5:c.1587G>A
|
ENSP00000465139.1:p.Ser529=
|
|
ENST00000593119.5:c.1785G>A
|
ENSP00000468541.1:p.Ser595=
|
|
NM_001276479.1:c.1785G>A
|
NP_001263408.1:p.Ser595=
|
|
NM_001276480.1:c.1389G>A
|
NP_001263409.1:p.Ser463=
|
|
NM_004793.3:c.1977G>A
|
NP_004784.2:p.Ser659=
|
|
NR_076392.1:n.1801G>A
|
|
|
NM_001276479.2:c.1785G>A
|
NP_001263408.1:p.Ser595=
|
|
NM_004793.4:c.1977G>A
MANE Select
|
NP_004784.2:p.Ser659=
|
|
NR_076392.2:n.1782G>A
|
|
|