ENST00000296292.8:c.159G>T
MANE Select
|
ENSP00000296292.3:p.Leu53=
|
|
ENST00000296292.7:c.159G>T
|
ENSP00000296292.3:p.Leu53=
|
|
ENST00000394738.7:c.150-1268G>T
|
ENSP00000378223.3:n.150-1268G>T
|
|
ENST00000467048.1:c.159G>T
|
ENSP00000420325.1:p.Leu53=
|
|
NM_052859.3:c.159G>T
|
NP_443091.1:p.Leu53=
|
|
XM_005265537.3:c.159G>T
|
XP_005265594.1:p.Leu53=
|
|
XM_006713384.2:c.159G>T
|
XP_006713447.1:p.Leu53=
|
|
XM_011534214.1:c.159G>T
|
XP_011532516.1:p.Leu53=
|
|
XM_011534215.1:c.159G>T
|
XP_011532517.1:p.Leu53=
|
|
XR_940507.1:n.218G>T
|
|
|
XM_005265537.4:c.159G>T
|
XP_005265594.1:p.Leu53=
|
|
XM_006713384.3:c.159G>T
|
XP_006713447.1:p.Leu53=
|
|
XM_011534214.2:c.159G>T
|
XP_011532516.1:p.Leu53=
|
|
XM_011534215.3:c.159G>T
|
XP_011532517.1:p.Leu53=
|
|
XM_011534216.3:c.-682G>T
|
XP_011532518.1:n.-682G>T
|
|
XM_017007460.1:c.159G>T
|
XP_016862949.1:p.Leu53=
|
|
XM_017007461.2:c.-682G>T
|
XP_016862950.1:n.-682G>T
|
|
XR_001740360.2:n.225G>T
|
|
|
NM_052859.4:c.159G>T
MANE Select
|
NP_443091.1:p.Leu53=
|
|