ENST00000433473.8:c.892G>C
|
ENSP00000394863.4:p.Ala298Pro
|
|
ENST00000439754.6:c.823G>C
|
ENSP00000403207.2:p.Ala275Pro
|
|
ENST00000449045.7:c.586G>C
|
ENSP00000392293.2:p.Ala196Pro
|
|
ENST00000530076.6:c.238G>C
|
ENSP00000434007.1:p.Ala80Pro
|
|
ENST00000530704.6:c.*518G>C
|
ENSP00000431655.1:n.*518G>C
|
|
ENST00000641083.1:c.985G>C
|
|
|
ENST00000641236.1:n.1132G>C
|
|
|
ENST00000641319.1:c.*105G>C
|
ENSP00000493128.1:n.*105G>C
|
|
ENST00000641381.1:c.317G>C
|
|
|
ENST00000641471.1:c.982G>C
|
ENSP00000493146.1:p.Ala328Pro
|
|
ENST00000641691.1:c.*747G>C
|
ENSP00000492910.1:n.*747G>C
|
|
ENST00000641924.1:c.*324G>C
|
ENSP00000493063.1:n.*324G>C
|
|
ENST00000642050.2:c.895G>C
MANE Select
|
ENSP00000493153.1:p.Ala299Pro
|
|
ENST00000372775.2:n.292G>C
|
|
|
ENST00000433473.7:c.895G>C
|
ENSP00000394863.3:p.Ala299Pro
|
|
ENST00000439754.5:c.508G>C
|
ENSP00000403207.1:p.Ala170Pro
|
|
ENST00000449045.6:c.586G>C
|
ENSP00000392293.2:p.Ala196Pro
|
|
ENST00000529905.5:c.895G>C
|
ENSP00000432053.1:p.Ala299Pro
|
|
ENST00000530076.5:c.238G>C
|
ENSP00000434007.1:p.Ala80Pro
|
|
ENST00000530704.5:c.*518G>C
|
ENSP00000431655.1:n.*518G>C
|
|
NM_000310.3:c.895G>C , LRG_690t1:c.895G>C
|
NP_000301.1:p.Ala299Pro
|
|
NM_001142604.1:c.586G>C
|
NP_001136076.1:p.Ala196Pro
|
|
XM_005271008.1:c.823G>C
|
XP_005271065.1:p.Ala275Pro
|
|
NM_001363695.1:c.823G>C
|
NP_001350624.1:p.Ala275Pro
|
|
NM_000310.4:c.895G>C
MANE Select
|
NP_000301.1:p.Ala299Pro
|
|
NM_001142604.2:c.586G>C
|
NP_001136076.1:p.Ala196Pro
|
|
NM_001363695.2:c.823G>C
|
NP_001350624.1:p.Ala275Pro
|
|