|
ENST00000234071.8:c.1097C>T
MANE Select
|
ENSP00000234071.4:p.Pro366Leu
|
|
|
ENST00000234071.7:c.1097C>T
|
ENSP00000234071.3:p.Pro366Leu
|
|
|
ENST00000402125.2:c.421C>T
|
|
|
|
ENST00000409048.1:c.1199C>T
|
ENSP00000386679.1:p.Pro400Leu
|
|
|
NM_000312.3:c.1097C>T , LRG_599t1:c.1097C>T
|
NP_000303.1:p.Pro366Leu
|
|
|
XM_005263715.3:c.1280C>T
|
XP_005263772.1:p.Pro427Leu
|
|
|
XM_005263716.3:c.1262C>T
|
XP_005263773.1:p.Pro421Leu
|
|
|
XM_005263717.3:c.1160C>T
|
XP_005263774.1:p.Pro387Leu
|
|
|
XR_923313.1:n.1332-393G>A
|
|
|
|
XM_005263717.4:c.1160C>T
|
XP_005263774.1:p.Pro387Leu
|
|
|
XM_017004505.1:c.1340C>T
|
XP_016859994.1:p.Pro447Leu
|
|
|
XM_024453002.1:c.1442C>T
|
XP_024308770.1:p.Pro481Leu
|
|
|
XM_024453003.1:c.1382C>T
|
XP_024308771.1:p.Pro461Leu
|
|
|
XM_024453004.1:c.1280C>T
|
XP_024308772.1:p.Pro427Leu
|
|
|
XM_024453005.1:c.1262C>T
|
XP_024308773.1:p.Pro421Leu
|
|
|
XM_024453006.1:c.1199C>T
|
XP_024308774.1:p.Pro400Leu
|
|
|
XR_001739705.1:n.3607-393G>A
|
|
|
|
XR_923313.2:n.4043-393G>A
|
|
|
|
NM_000312.4:c.1097C>T
MANE Select
|
NP_000303.1:p.Pro366Leu
|
|
|
NM_001375602.1:c.1280C>T
|
NP_001362531.1:p.Pro427Leu
|
|
|
NM_001375603.1:c.1262C>T
|
NP_001362532.1:p.Pro421Leu
|
|
|
NM_001375604.1:c.1160C>T
|
NP_001362533.1:p.Pro387Leu
|
|
|
NM_001375605.1:c.1199C>T
|
NP_001362534.1:p.Pro400Leu
|
|
|
NM_001375606.1:c.1265C>T
|
NP_001362535.1:p.Pro422Leu
|
|
|
NM_001375607.1:c.1283C>T
|
NP_001362536.1:p.Pro428Leu
|
|
|
NM_001375608.1:c.1040C>T
|
NP_001362537.1:p.Pro347Leu
|
|
|
NM_001375609.1:c.1073C>T
|
NP_001362538.1:p.Pro358Leu
|
|
|
NM_001375610.1:c.1091C>T
|
NP_001362539.1:p.Pro364Leu
|
|
|
NM_001375611.1:c.1097C>T
|
NP_001362540.1:p.Pro366Leu
|
|
|
NM_001375613.1:c.1097C>T
|
NP_001362542.1:p.Pro366Leu
|
|
