ENST00000310581.10:c.2586G>T
MANE Select
|
ENSP00000309572.5:p.Leu862=
|
|
ENST00000656021.1:c.*2132G>T
|
ENSP00000499759.1:n.*2132G>T
|
|
ENST00000310581.9:c.2586G>T
|
ENSP00000309572.5:p.Leu862=
|
|
ENST00000334602.10:c.2586G>T
|
ENSP00000334346.6:p.Leu862=
|
|
ENST00000460137.6:c.2368G>T
|
ENSP00000425003.1:p.Ala790Ser
|
|
ENST00000484238.6:n.1217G>T
|
|
|
ENST00000508104.2:c.2404G>T
|
ENSP00000426042.2:p.Ala802Ser
|
|
NM_001193376.1:c.2586G>T
|
NP_001180305.1:p.Leu862=
|
|
NM_198253.2:c.2586G>T , LRG_343t1:c.2586G>T
|
NP_937983.2:p.Leu862=
|
|
XM_011514104.1:c.1056G>T
|
XP_011512406.1:p.Leu352=
|
|
XM_011514105.1:c.942G>T
|
XP_011512407.1:p.Leu314=
|
|
XM_011514106.1:c.942G>T
|
XP_011512408.1:p.Leu314=
|
|
NR_149162.1:n.2462G>T
|
|
|
NR_149163.1:n.2426G>T
|
|
|
NM_001193376.2:c.2586G>T
|
NP_001180305.1:p.Leu862=
|
|
NM_198253.3:c.2586G>T
MANE Select
|
NP_937983.2:p.Leu862=
|
|
NR_149162.2:n.2483G>T
|
|
|
NR_149163.2:n.2447G>T
|
|
|
NM_001193376.3:c.2586G>T
|
NP_001180305.1:p.Leu862=
|
|
NR_149162.3:n.2483G>T
|
|
|
NR_149163.3:n.2447G>T
|
|
|