ENST00000265104.5:c.10894T>C
MANE Select
|
ENSP00000265104.4:p.Tyr3632His
|
|
ENST00000681290.1:c.10849T>C
|
ENSP00000505288.1:p.Tyr3617His
|
|
ENST00000265104.4:c.10894T>C
|
ENSP00000265104.4:p.Tyr3632His
|
|
NM_001369.2:c.10894T>C
|
NP_001360.1:p.Tyr3632His
|
|
XM_005248262.2:c.10849T>C
|
XP_005248319.1:p.Tyr3617His
|
|
XM_005248262.3:c.11002T>C
|
XP_005248319.2:p.Tyr3668His
|
|
XM_017009177.1:c.11002T>C
|
XP_016864666.1:p.Tyr3668His
|
|
XM_017009178.1:c.9907T>C
|
XP_016864667.1:p.Tyr3303His
|
|
XM_017009179.2:c.9907T>C
|
XP_016864668.1:p.Tyr3303His
|
|
XM_017009180.1:c.11002T>C
|
XP_016864669.1:p.Tyr3668His
|
|
XM_017009181.1:c.11002T>C
|
XP_016864670.1:p.Tyr3668His
|
|
XM_017009182.1:c.11002T>C
|
XP_016864671.1:p.Tyr3668His
|
|
XM_017009185.1:c.6091T>C
|
XP_016864674.1:p.Tyr2031His
|
|
XM_017009186.1:c.5644T>C
|
XP_016864675.1:p.Tyr1882His
|
|
XM_017009188.1:c.4981T>C
|
XP_016864677.1:p.Tyr1661His
|
|
XM_024454388.1:c.9907T>C
|
XP_024310156.1:p.Tyr3303His
|
|
XM_024454389.1:c.9496T>C
|
XP_024310157.1:p.Tyr3166His
|
|
NM_001369.3:c.10894T>C
MANE Select
|
NP_001360.1:p.Tyr3632His
|
|