ENST00000684880.1:c.*43T>C
|
ENSP00000510280.1:n.*43T>C
|
|
ENST00000689310.1:c.407T>C
|
ENSP00000510438.1:p.Val136Ala
|
|
ENST00000692630.1:n.585T>C
|
|
|
ENST00000370818.8:c.455T>C
MANE Select
|
ENSP00000359854.3:p.Val152Ala
|
|
ENST00000394299.7:c.455T>C
|
ENSP00000377836.2:p.Val152Ala
|
|
ENST00000370818.7:c.455T>C
|
ENSP00000359854.3:p.Val152Ala
|
|
ENST00000394299.6:c.455T>C
|
ENSP00000377836.2:p.Val152Ala
|
|
ENST00000631057.2:c.293T>C
|
ENSP00000486325.1:p.Val98Ala
|
|
NM_001164617.1:c.455T>C
|
NP_001158089.1:p.Val152Ala
|
|
NM_001164618.1:c.407T>C
|
NP_001158090.1:p.Val136Ala
|
|
NM_001164619.1:c.293T>C
|
NP_001158091.1:p.Val98Ala
|
|
NM_004484.3:c.455T>C , LRG_505t1:c.455T>C
|
NP_004475.1:p.Val152Ala
|
|
XM_017029413.2:c.455T>C
|
XP_016884902.1:p.Val152Ala
|
|
NM_001164617.2:c.455T>C
|
NP_001158089.1:p.Val152Ala
|
|
NM_001164618.2:c.407T>C
|
NP_001158090.1:p.Val136Ala
|
|
NM_001164619.2:c.293T>C
|
NP_001158091.1:p.Val98Ala
|
|
NM_004484.4:c.455T>C
MANE Select
|
NP_004475.1:p.Val152Ala
|
|