ENST00000422737.7:c.4344T=
|
ENSP00000415650.3:p.Leu1448=
|
|
ENST00000457135.2:c.553T=
|
|
|
ENST00000334344.11:c.4344T=
MANE Select
|
ENSP00000335044.6:p.Leu1448=
|
|
ENST00000422737.6:c.4265T=
|
|
|
ENST00000334344.10:c.4344T=
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ENSP00000335044.6:p.Leu1448=
|
|
ENST00000422737.5:c.3897T=
|
ENSP00000415650.1:p.Leu1299=
|
|
ENST00000444670.5:c.3174T=
|
ENSP00000397307.1:p.Leu1058=
|
|
ENST00000457135.1:c.168T=
|
ENSP00000388357.1:p.Leu56=
|
|
ENST00000479608.5:n.3635T=
|
|
|
NM_152641.2:c.4344T=
|
NP_689854.2:p.Leu1448=
|
|
XM_006719272.2:c.4344T=
|
XP_006719335.1:p.Leu1448=
|
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XM_011538025.1:c.2712T=
|
XP_011536327.1:p.Leu904=
|
|
XR_944505.1:n.4492T=
|
|
|
NM_001347839.1:c.4344T=
|
NP_001334768.1:p.Leu1448=
|
|
NM_152641.3:c.4344T=
|
NP_689854.2:p.Leu1448=
|
|
XM_006719272.4:c.4344T=
|
XP_006719335.1:p.Leu1448=
|
|
XR_944505.3:n.4475T=
|
|
|
NM_152641.4:c.4344T=
MANE Select
|
NP_689854.2:p.Leu1448=
|
|
NM_001347839.2:c.4344T=
|
NP_001334768.1:p.Leu1448=
|
|