ENST00000683090.1:n.1314T>G
|
|
|
ENST00000265104.5:c.6383T>G
MANE Select
|
ENSP00000265104.4:p.Val2128Gly
|
|
ENST00000681290.1:c.6338T>G
|
ENSP00000505288.1:p.Val2113Gly
|
|
ENST00000265104.4:c.6383T>G
|
ENSP00000265104.4:p.Val2128Gly
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|
NM_001369.2:c.6383T>G
|
NP_001360.1:p.Val2128Gly
|
|
XM_005248262.2:c.6338T>G
|
XP_005248319.1:p.Val2113Gly
|
|
XM_011513990.1:c.6383T>G
|
XP_011512292.1:p.Val2128Gly
|
|
XR_925598.1:n.6590T>G
|
|
|
XM_005248262.3:c.6491T>G
|
XP_005248319.2:p.Val2164Gly
|
|
XM_017009177.1:c.6491T>G
|
XP_016864666.1:p.Val2164Gly
|
|
XM_017009178.1:c.5396T>G
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XP_016864667.1:p.Val1799Gly
|
|
XM_017009179.2:c.5396T>G
|
XP_016864668.1:p.Val1799Gly
|
|
XM_017009180.1:c.6491T>G
|
XP_016864669.1:p.Val2164Gly
|
|
XM_017009181.1:c.6491T>G
|
XP_016864670.1:p.Val2164Gly
|
|
XM_017009182.1:c.6491T>G
|
XP_016864671.1:p.Val2164Gly
|
|
XM_017009183.1:c.6491T>G
|
XP_016864672.1:p.Val2164Gly
|
|
XM_017009184.1:c.6491T>G
|
XP_016864673.1:p.Val2164Gly
|
|
XM_017009185.1:c.1580T>G
|
XP_016864674.1:p.Val527Gly
|
|
XM_017009186.1:c.1133T>G
|
XP_016864675.1:p.Val378Gly
|
|
XM_017009187.1:c.6491T>G
|
XP_016864676.1:p.Val2164Gly
|
|
XM_017009188.1:c.470T>G
|
XP_016864677.1:p.Val157Gly
|
|
XM_024454388.1:c.5396T>G
|
XP_024310156.1:p.Val1799Gly
|
|
XM_024454389.1:c.4985T>G
|
XP_024310157.1:p.Val1662Gly
|
|
XR_001742034.1:n.6508T>G
|
|
|
XR_001742035.1:n.6508T>G
|
|
|
NM_001369.3:c.6383T>G
MANE Select
|
NP_001360.1:p.Val2128Gly
|
|