ENST00000368845.6:c.1118G>T
MANE Select
|
ENSP00000357838.5:p.Gly373Val
|
|
ENST00000368845.5:c.1118G>T
|
ENSP00000357838.5:p.Gly373Val
|
|
ENST00000471127.1:n.628G>T
|
|
|
ENST00000539214.5:c.704G>T
|
ENSP00000439042.1:p.Gly235Val
|
|
NM_000274.3:c.1118G>T , LRG_685t1:c.1118G>T
|
NP_000265.1:p.Gly373Val
|
|
NM_001171814.1:c.704G>T
|
NP_001165285.1:p.Gly235Val
|
|
XM_006717871.2:c.1118G>T
|
XP_006717934.1:p.Gly373Val
|
|
XM_011539833.1:c.1118G>T
|
XP_011538135.1:p.Gly373Val
|
|
XM_011539834.1:c.1118G>T
|
XP_011538136.1:p.Gly373Val
|
|
NM_001322965.1:c.1118G>T
|
NP_001309894.1:p.Gly373Val
|
|
NM_001322966.1:c.1118G>T
|
NP_001309895.1:p.Gly373Val
|
|
NM_001322967.1:c.1118G>T
|
NP_001309896.1:p.Gly373Val
|
|
NM_001322968.1:c.1118G>T
|
NP_001309897.1:p.Gly373Val
|
|
NM_001322969.1:c.1118G>T
|
NP_001309898.1:p.Gly373Val
|
|
NM_001322970.1:c.1118G>T
|
NP_001309899.1:p.Gly373Val
|
|
NM_001322971.1:c.797G>T
|
NP_001309900.1:p.Gly266Val
|
|
NM_001322974.1:c.518G>T
|
NP_001309903.1:p.Gly173Val
|
|
XM_017016279.1:c.518G>T
|
XP_016871768.1:p.Gly173Val
|
|
NM_000274.4:c.1118G>T
MANE Select
|
NP_000265.1:p.Gly373Val
|
|
NM_001322965.2:c.1118G>T
|
NP_001309894.1:p.Gly373Val
|
|
NM_001322966.2:c.1118G>T
|
NP_001309895.1:p.Gly373Val
|
|
NM_001322967.2:c.1118G>T
|
NP_001309896.1:p.Gly373Val
|
|
NM_001322968.2:c.1118G>T
|
NP_001309897.1:p.Gly373Val
|
|
NM_001322969.2:c.1118G>T
|
NP_001309898.1:p.Gly373Val
|
|
NM_001322970.2:c.1118G>T
|
NP_001309899.1:p.Gly373Val
|
|
NM_001322971.2:c.797G>T
|
NP_001309900.1:p.Gly266Val
|
|
NM_001322974.2:c.518G>T
|
NP_001309903.1:p.Gly173Val
|
|
NM_001171814.2:c.704G>T
|
NP_001165285.1:p.Gly235Val
|
|