ENST00000473665.2:n.5213G>C
|
|
|
ENST00000482662.2:n.3620G>C
|
|
|
ENST00000685865.1:n.1572G>C
|
|
|
ENST00000687250.1:n.1272G>C
|
|
|
ENST00000687995.1:n.1521G>C
|
|
|
ENST00000688205.1:c.*762G>C
|
ENSP00000509673.1:n.*762G>C
|
|
ENST00000688788.1:n.1408G>C
|
|
|
ENST00000689276.1:c.1100G>C
|
ENSP00000510012.1:p.Trp367Ser
|
|
ENST00000689576.1:c.1169G>C
|
ENSP00000508712.1:p.Trp390Ser
|
|
ENST00000690108.1:c.*825G>C
|
ENSP00000510617.1:n.*825G>C
|
|
ENST00000690468.1:c.890G>C
|
ENSP00000509078.1:p.Trp297Ser
|
|
ENST00000690595.1:c.494G>C
|
ENSP00000508979.1:p.Trp165Ser
|
|
ENST00000691348.1:c.998G>C
|
ENSP00000509369.1:p.Trp333Ser
|
|
ENST00000691410.1:c.*746G>C
|
ENSP00000508479.1:n.*746G>C
|
|
ENST00000693287.1:c.485G>C
|
ENSP00000510264.1:p.Trp162Ser
|
|
ENST00000693681.1:c.482G>C
|
ENSP00000510789.1:p.Trp161Ser
|
|
ENST00000233838.9:c.1169G>C
MANE Select
|
ENSP00000233838.3:p.Trp390Ser
|
|
ENST00000233838.8:c.1169G>C
|
ENSP00000233838.3:p.Trp390Ser
|
|
ENST00000430215.7:c.998G>C
|
ENSP00000408045.3:p.Trp333Ser
|
|
ENST00000465637.5:n.179-5053G>C
|
|
|
ENST00000473665.1:n.662G>C
|
|
|
ENST00000482662.1:n.586G>C
|
|
|
NM_000821.5:c.1169G>C
|
NP_000812.2:p.Trp390Ser
|
|
NM_000821.6:c.1169G>C
|
NP_000812.2:p.Trp390Ser
|
|
NM_001142269.2:c.998G>C
|
NP_001135741.1:p.Trp333Ser
|
|
NM_001142269.3:c.998G>C
|
NP_001135741.1:p.Trp333Ser
|
|
XM_005264259.3:c.1169G>C
|
XP_005264316.1:p.Trp390Ser
|
|
XM_011532764.1:c.347G>C
|
XP_011531066.1:p.Trp116Ser
|
|
XM_011532765.1:c.347G>C
|
XP_011531067.1:p.Trp116Ser
|
|
XR_939677.1:n.1234G>C
|
|
|
XM_005264259.5:c.1169G>C
|
XP_005264316.1:p.Trp390Ser
|
|
XM_011532764.3:c.347G>C
|
XP_011531066.1:p.Trp116Ser
|
|
XM_011532765.3:c.347G>C
|
XP_011531067.1:p.Trp116Ser
|
|
XM_017003803.2:c.998G>C
|
XP_016859292.1:p.Trp333Ser
|
|
XR_001738703.2:n.1234G>C
|
|
|
NM_000821.7:c.1169G>C
MANE Select
|
NP_000812.2:p.Trp390Ser
|
|
NM_001142269.4:c.998G>C
|
NP_001135741.1:p.Trp333Ser
|
|