ENST00000234071.8:c.558C>A
MANE Select
|
ENSP00000234071.4:p.Pro186=
|
|
ENST00000234071.7:c.558C>A
|
ENSP00000234071.3:p.Pro186=
|
|
ENST00000402125.2:c.121-2250C>A
|
|
|
ENST00000409048.1:c.660C>A
|
ENSP00000386679.1:p.Pro220=
|
|
ENST00000442644.5:c.501C>A
|
ENSP00000411241.1:p.Pro167=
|
|
ENST00000464089.1:n.144C>A
|
|
|
NM_000312.3:c.558C>A , LRG_599t1:c.558C>A
|
NP_000303.1:p.Pro186=
|
|
XM_005263715.3:c.741C>A
|
XP_005263772.1:p.Pro247=
|
|
XM_005263716.3:c.723C>A
|
XP_005263773.1:p.Pro241=
|
|
XM_005263717.3:c.621C>A
|
XP_005263774.1:p.Pro207=
|
|
XM_005263717.4:c.621C>A
|
XP_005263774.1:p.Pro207=
|
|
XM_017004505.1:c.801C>A
|
XP_016859994.1:p.Pro267=
|
|
XM_024453002.1:c.903C>A
|
XP_024308770.1:p.Pro301=
|
|
XM_024453003.1:c.843C>A
|
XP_024308771.1:p.Pro281=
|
|
XM_024453004.1:c.741C>A
|
XP_024308772.1:p.Pro247=
|
|
XM_024453005.1:c.723C>A
|
XP_024308773.1:p.Pro241=
|
|
XM_024453006.1:c.660C>A
|
XP_024308774.1:p.Pro220=
|
|
XR_923313.2:n.4478G>T
|
|
|
NM_000312.4:c.558C>A
MANE Select
|
NP_000303.1:p.Pro186=
|
|
NM_001375602.1:c.741C>A
|
NP_001362531.1:p.Pro247=
|
|
NM_001375603.1:c.723C>A
|
NP_001362532.1:p.Pro241=
|
|
NM_001375604.1:c.621C>A
|
NP_001362533.1:p.Pro207=
|
|
NM_001375605.1:c.660C>A
|
NP_001362534.1:p.Pro220=
|
|
NM_001375606.1:c.726C>A
|
NP_001362535.1:p.Pro242=
|
|
NM_001375607.1:c.744C>A
|
NP_001362536.1:p.Pro248=
|
|
NM_001375608.1:c.501C>A
|
NP_001362537.1:p.Pro167=
|
|
NM_001375609.1:c.534C>A
|
NP_001362538.1:p.Pro178=
|
|
NM_001375610.1:c.552C>A
|
NP_001362539.1:p.Pro184=
|
|
NM_001375611.1:c.558C>A
|
NP_001362540.1:p.Pro186=
|
|
NM_001375613.1:c.558C>A
|
NP_001362542.1:p.Pro186=
|
|