ENST00000265104.5:c.5396C>G
MANE Select
|
ENSP00000265104.4:p.Ser1799Ter
|
|
ENST00000681290.1:c.5351C>G
|
ENSP00000505288.1:p.Ser1784Ter
|
|
ENST00000265104.4:c.5396C>G
|
ENSP00000265104.4:p.Ser1799Ter
|
|
NM_001369.2:c.5396C>G
|
NP_001360.1:p.Ser1799Ter
|
|
XM_005248262.2:c.5351C>G
|
XP_005248319.1:p.Ser1784Ter
|
|
XM_011513990.1:c.5396C>G
|
XP_011512292.1:p.Ser1799Ter
|
|
XR_925598.1:n.5603C>G
|
|
|
XM_005248262.3:c.5504C>G
|
XP_005248319.2:p.Ser1835Ter
|
|
XM_017009177.1:c.5504C>G
|
XP_016864666.1:p.Ser1835Ter
|
|
XM_017009178.1:c.4409C>G
|
XP_016864667.1:p.Ser1470Ter
|
|
XM_017009179.2:c.4409C>G
|
XP_016864668.1:p.Ser1470Ter
|
|
XM_017009180.1:c.5504C>G
|
XP_016864669.1:p.Ser1835Ter
|
|
XM_017009181.1:c.5504C>G
|
XP_016864670.1:p.Ser1835Ter
|
|
XM_017009182.1:c.5504C>G
|
XP_016864671.1:p.Ser1835Ter
|
|
XM_017009183.1:c.5504C>G
|
XP_016864672.1:p.Ser1835Ter
|
|
XM_017009184.1:c.5504C>G
|
XP_016864673.1:p.Ser1835Ter
|
|
XM_017009185.1:c.593C>G
|
XP_016864674.1:p.Ser198Ter
|
|
XM_017009186.1:c.146C>G
|
XP_016864675.1:p.Ser49Ter
|
|
XM_017009187.1:c.5504C>G
|
XP_016864676.1:p.Ser1835Ter
|
|
XM_024454388.1:c.4409C>G
|
XP_024310156.1:p.Ser1470Ter
|
|
XM_024454389.1:c.3998C>G
|
XP_024310157.1:p.Ser1333Ter
|
|
XR_001742034.1:n.5521C>G
|
|
|
XR_001742035.1:n.5521C>G
|
|
|
NM_001369.3:c.5396C>G
MANE Select
|
NP_001360.1:p.Ser1799Ter
|
|