ENST00000624552.4:c.14906T>G
|
ENSP00000485357.2:p.Leu4969Arg
|
|
ENST00000683500.2:c.14963T>G
MANE Select
|
ENSP00000508292.2:p.Leu4988Arg
|
|
ENST00000623487.1:n.3309T>G
|
|
|
ENST00000624552.3:c.14903T>G
|
ENSP00000485357.1:p.Leu4968Arg
|
|
NM_001291815.1:c.14963T>G
|
NP_001278744.1:p.Leu4988Arg
|
|
XM_011518465.1:c.14840T>G
|
XP_011516767.1:p.Leu4947Arg
|
|
XM_011518466.1:c.14831T>G
|
XP_011516768.1:p.Leu4944Arg
|
|
XM_011518467.1:c.14786T>G
|
XP_011516769.1:p.Leu4929Arg
|
|
NM_001291815.2:c.14963T>G
MANE Select
|
NP_001278744.1:p.Leu4988Arg
|
|
XM_011518465.2:c.14840T>G
|
XP_011516767.1:p.Leu4947Arg
|
|
XM_011518466.2:c.14831T>G
|
XP_011516768.1:p.Leu4944Arg
|
|
XM_011518467.2:c.14786T>G
|
XP_011516769.1:p.Leu4929Arg
|
|
XM_017014585.1:c.11744T>G
|
XP_016870074.1:p.Leu3915Arg
|
|
XM_017014586.1:c.7541T>G
|
XP_016870075.1:p.Leu2514Arg
|
|
XR_001746957.1:n.92+205A>C
|
|
|
XR_001746958.1:n.92+205A>C
|
|
|