ENST00000703118.1:c.4357C>G
|
ENSP00000515181.1:p.Leu1453Val
|
|
ENST00000703131.1:n.277C>G
|
|
|
ENST00000703140.1:c.4144C>G
|
ENSP00000515197.1:p.Leu1382Val
|
|
ENST00000703141.1:c.4357C>G
|
ENSP00000515198.1:p.Leu1453Val
|
|
ENST00000703142.1:c.*1187C>G
|
ENSP00000515199.1:n.*1187C>G
|
|
ENST00000361445.9:c.4357C>G
MANE Select
|
ENSP00000354558.4:p.Leu1453Val
|
|
ENST00000361445.8:c.4357C>G
|
ENSP00000354558.4:p.Leu1453Val
|
|
NM_004958.3:c.4357C>G , LRG_734t1:c.4357C>G
|
NP_004949.1:p.Leu1453Val
|
|
XM_005263438.1:c.4357C>G
|
XP_005263495.1:p.Leu1453Val
|
|
XM_011541166.1:c.4357C>G
|
XP_011539468.1:p.Leu1453Val
|
|
XR_244786.1:n.4478C>G
|
|
|
XM_005263438.2:c.4357C>G
|
XP_005263495.1:p.Leu1453Val
|
|
XM_011541166.2:c.4357C>G
|
XP_011539468.1:p.Leu1453Val
|
|
XM_017000900.1:c.3676C>G
|
XP_016856389.1:p.Leu1226Val
|
|
XM_017000901.1:c.3109C>G
|
XP_016856390.1:p.Leu1037Val
|
|
XM_024446187.1:c.4357C>G
|
XP_024301955.1:p.Leu1453Val
|
|
XR_001737087.1:n.4478C>G
|
|
|
NM_004958.4:c.4357C>G
MANE Select
|
NP_004949.1:p.Leu1453Val
|
|
NM_001386500.1:c.4357C>G
|
NP_001373429.1:p.Leu1453Val
|
|
NM_001386501.1:c.3109C>G
|
NP_001373430.1:p.Leu1037Val
|
|