ENST00000310581.10:c.2953C>T
MANE Select
|
ENSP00000309572.5:p.Leu985=
|
|
ENST00000656021.1:c.*2499C>T
|
ENSP00000499759.1:n.*2499C>T
|
|
ENST00000667927.1:n.241C>T
|
|
|
ENST00000310581.9:c.2953C>T
|
ENSP00000309572.5:p.Leu985=
|
|
ENST00000334602.10:c.2764C>T
|
ENSP00000334346.6:p.Leu922=
|
|
ENST00000460137.6:c.2546C>T
|
ENSP00000425003.1:n.2546C>T
|
|
ENST00000484238.6:n.1395C>T
|
|
|
NM_001193376.1:c.2764C>T
|
NP_001180305.1:p.Leu922=
|
|
NM_198253.2:c.2953C>T , LRG_343t1:c.2953C>T
|
NP_937983.2:p.Leu985=
|
|
XM_011514104.1:c.1423C>T
|
XP_011512406.1:p.Leu475=
|
|
XM_011514105.1:c.1309C>T
|
XP_011512407.1:p.Leu437=
|
|
XM_011514106.1:c.1309C>T
|
XP_011512408.1:p.Leu437=
|
|
NR_149162.1:n.2640C>T
|
|
|
NR_149163.1:n.2604C>T
|
|
|
NM_001193376.2:c.2764C>T
|
NP_001180305.1:p.Leu922=
|
|
NM_198253.3:c.2953C>T
MANE Select
|
NP_937983.2:p.Leu985=
|
|
NR_149162.2:n.2661C>T
|
|
|
NR_149163.2:n.2625C>T
|
|
|
NM_001193376.3:c.2764C>T
|
NP_001180305.1:p.Leu922=
|
|
NR_149162.3:n.2661C>T
|
|
|
NR_149163.3:n.2625C>T
|
|
|