ENST00000234071.8:c.588C>T
MANE Select
|
ENSP00000234071.4:p.His196=
|
|
ENST00000234071.7:c.588C>T
|
ENSP00000234071.3:p.His196=
|
|
ENST00000402125.2:c.121-2220C>T
|
|
|
ENST00000409048.1:c.690C>T
|
ENSP00000386679.1:p.His230=
|
|
ENST00000464089.1:n.174C>T
|
|
|
NM_000312.3:c.588C>T , LRG_599t1:c.588C>T
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NP_000303.1:p.His196=
|
|
XM_005263715.3:c.771C>T
|
XP_005263772.1:p.His257=
|
|
XM_005263716.3:c.753C>T
|
XP_005263773.1:p.His251=
|
|
XM_005263717.3:c.651C>T
|
XP_005263774.1:p.His217=
|
|
XM_005263717.4:c.651C>T
|
XP_005263774.1:p.His217=
|
|
XM_017004505.1:c.831C>T
|
XP_016859994.1:p.His277=
|
|
XM_024453002.1:c.933C>T
|
XP_024308770.1:p.His311=
|
|
XM_024453003.1:c.873C>T
|
XP_024308771.1:p.His291=
|
|
XM_024453004.1:c.771C>T
|
XP_024308772.1:p.His257=
|
|
XM_024453005.1:c.753C>T
|
XP_024308773.1:p.His251=
|
|
XM_024453006.1:c.690C>T
|
XP_024308774.1:p.His230=
|
|
XR_923313.2:n.4448G>A
|
|
|
NM_000312.4:c.588C>T
MANE Select
|
NP_000303.1:p.His196=
|
|
NM_001375602.1:c.771C>T
|
NP_001362531.1:p.His257=
|
|
NM_001375603.1:c.753C>T
|
NP_001362532.1:p.His251=
|
|
NM_001375604.1:c.651C>T
|
NP_001362533.1:p.His217=
|
|
NM_001375605.1:c.690C>T
|
NP_001362534.1:p.His230=
|
|
NM_001375606.1:c.756C>T
|
NP_001362535.1:p.His252=
|
|
NM_001375607.1:c.774C>T
|
NP_001362536.1:p.His258=
|
|
NM_001375608.1:c.531C>T
|
NP_001362537.1:p.His177=
|
|
NM_001375609.1:c.564C>T
|
NP_001362538.1:p.His188=
|
|
NM_001375610.1:c.582C>T
|
NP_001362539.1:p.His194=
|
|
NM_001375611.1:c.588C>T
|
NP_001362540.1:p.His196=
|
|
NM_001375613.1:c.588C>T
|
NP_001362542.1:p.His196=
|
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