ENST00000624552.4:c.14903T>G
|
ENSP00000485357.2:p.Leu4968Arg
|
|
ENST00000683500.2:c.14960T>G
MANE Select
|
ENSP00000508292.2:p.Leu4987Arg
|
|
ENST00000623487.1:n.3306T>G
|
|
|
ENST00000624552.3:c.14900T>G
|
ENSP00000485357.1:p.Leu4967Arg
|
|
NM_001291815.1:c.14960T>G
|
NP_001278744.1:p.Leu4987Arg
|
|
XM_011518465.1:c.14837T>G
|
XP_011516767.1:p.Leu4946Arg
|
|
XM_011518466.1:c.14828T>G
|
XP_011516768.1:p.Leu4943Arg
|
|
XM_011518467.1:c.14783T>G
|
XP_011516769.1:p.Leu4928Arg
|
|
NM_001291815.2:c.14960T>G
MANE Select
|
NP_001278744.1:p.Leu4987Arg
|
|
XM_011518465.2:c.14837T>G
|
XP_011516767.1:p.Leu4946Arg
|
|
XM_011518466.2:c.14828T>G
|
XP_011516768.1:p.Leu4943Arg
|
|
XM_011518467.2:c.14783T>G
|
XP_011516769.1:p.Leu4928Arg
|
|
XM_017014585.1:c.11741T>G
|
XP_016870074.1:p.Leu3914Arg
|
|
XM_017014586.1:c.7538T>G
|
XP_016870075.1:p.Leu2513Arg
|
|
XR_001746957.1:n.92+208A>C
|
|
|
XR_001746958.1:n.92+208A>C
|
|
|