ENST00000680213.2:n.1540T>G
|
|
|
ENST00000682376.1:n.5713T>G
|
|
|
ENST00000683011.1:n.1423T>G
|
|
|
ENST00000683967.1:n.3849T>G
|
|
|
ENST00000684013.1:n.2144T>G
|
|
|
ENST00000684099.1:n.2140T>G
|
|
|
ENST00000265104.5:c.1484T>G
MANE Select
|
ENSP00000265104.4:p.Val495Gly
|
|
ENST00000680213.1:c.1244T>G
|
ENSP00000506622.1:p.Val415Gly
|
|
ENST00000681290.1:c.1439T>G
|
ENSP00000505288.1:p.Val480Gly
|
|
ENST00000265104.4:c.1484T>G
|
ENSP00000265104.4:p.Val495Gly
|
|
ENST00000508040.1:n.1892T>G
|
|
|
NM_001369.2:c.1484T>G
|
NP_001360.1:p.Val495Gly
|
|
XM_005248262.2:c.1439T>G
|
XP_005248319.1:p.Val480Gly
|
|
XM_011513990.1:c.1484T>G
|
XP_011512292.1:p.Val495Gly
|
|
XR_925598.1:n.1691T>G
|
|
|
XM_005248262.3:c.1592T>G
|
XP_005248319.2:p.Val531Gly
|
|
XM_017009177.1:c.1592T>G
|
XP_016864666.1:p.Val531Gly
|
|
XM_017009178.1:c.497T>G
|
XP_016864667.1:p.Val166Gly
|
|
XM_017009179.2:c.497T>G
|
XP_016864668.1:p.Val166Gly
|
|
XM_017009180.1:c.1592T>G
|
XP_016864669.1:p.Val531Gly
|
|
XM_017009181.1:c.1592T>G
|
XP_016864670.1:p.Val531Gly
|
|
XM_017009182.1:c.1592T>G
|
XP_016864671.1:p.Val531Gly
|
|
XM_017009183.1:c.1592T>G
|
XP_016864672.1:p.Val531Gly
|
|
XM_017009184.1:c.1592T>G
|
XP_016864673.1:p.Val531Gly
|
|
XM_017009187.1:c.1592T>G
|
XP_016864676.1:p.Val531Gly
|
|
XM_024454388.1:c.497T>G
|
XP_024310156.1:p.Val166Gly
|
|
XM_024454389.1:c.86T>G
|
XP_024310157.1:p.Val29Gly
|
|
XR_001742034.1:n.1609T>G
|
|
|
XR_001742035.1:n.1609T>G
|
|
|
NM_001369.3:c.1484T>G
MANE Select
|
NP_001360.1:p.Val495Gly
|
|