ENST00000642944.1:c.98G>T
|
ENSP00000495674.1:p.Gly33Val
|
|
ENST00000643023.1:c.272G>T
|
ENSP00000495664.1:p.Gly91Val
|
|
ENST00000643584.1:c.272G>T
|
ENSP00000494987.1:p.Gly91Val
|
|
ENST00000644338.1:c.272G>T
|
ENSP00000494723.1:p.Gly91Val
|
|
ENST00000646602.1:c.272G>T
|
ENSP00000495250.1:p.Gly91Val
|
|
ENST00000646804.1:c.98G>T
|
ENSP00000493977.1:p.Gly33Val
|
|
ENST00000646932.1:c.272G>T
MANE Select
|
ENSP00000494360.1:p.Gly91Val
|
|
ENST00000647361.1:c.*65G>T
|
ENSP00000494607.1:n.*65G>T
|
|
ENST00000378654.8:c.272G>T
|
ENSP00000367923.3:p.Gly91Val
|
|
ENST00000433022.1:c.90+12199G>T
|
ENSP00000415091.1:n.90+12199G>T
|
|
ENST00000434484.5:c.62G>T
|
ENSP00000392771.1:p.Gly21Val
|
|
ENST00000470760.2:c.272G>T
|
ENSP00000488974.1:p.Gly91Val
|
|
ENST00000497202.6:c.366G>T
|
ENSP00000489175.1:p.Arg122Ser
|
|
NM_003850.2:c.272G>T
|
NP_003841.1:p.Gly91Val
|
|
XM_011535292.1:c.35G>T
|
XP_011533594.1:p.Gly12Val
|
|
XM_011535293.1:c.-131G>T
|
XP_011533595.1:n.-131G>T
|
|
XR_941688.1:n.316G>T
|
|
|
NM_003850.3:c.272G>T
MANE Select
|
NP_003841.1:p.Gly91Val
|
|