|
ENST00000556892.6:c.182T>C
|
ENSP00000452206.2:p.Phe61Ser
|
|
|
ENST00000556979.6:c.*854T>C
|
ENSP00000452378.1:n.*854T>C
|
|
|
ENST00000358664.9:c.401T>C
MANE Select
|
ENSP00000351490.4:p.Phe134Ser
|
|
|
ENST00000651648.1:c.145-6189T>C
|
ENSP00000498863.1:n.145-6189T>C
|
|
|
ENST00000284165.10:c.*1245T>C
|
ENSP00000284165.6:n.*1245T>C
|
|
|
ENST00000341653.6:c.171+17150T>C
|
ENSP00000342482.2:n.171+17150T>C
|
|
|
ENST00000358402.8:c.374T>C
|
ENSP00000351175.4:p.Phe125Ser
|
|
|
ENST00000358664.8:c.401T>C
|
ENSP00000351490.4:p.Phe134Ser
|
|
|
ENST00000394606.6:c.*174T>C
|
ENSP00000378104.2:n.*174T>C
|
|
|
ENST00000553928.5:c.*190T>C
|
ENSP00000451907.1:n.*190T>C
|
|
|
ENST00000555419.5:c.293T>C
|
ENSP00000452405.1:p.Phe98Ser
|
|
|
ENST00000555932.5:c.142T>C
|
ENSP00000450763.1:p.Ser48Pro
|
|
|
ENST00000557277.5:c.212T>C
|
ENSP00000450955.1:p.Phe71Ser
|
|
|
ENST00000618858.4:c.*190T>C
|
ENSP00000480127.1:n.*190T>C
|
|
|
NM_001271069.1:c.144+17150T>C
|
NP_001257998.1:n.144+17150T>C
|
|
|
NM_002382.4:c.401T>C
|
NP_002373.3:p.Phe134Ser
|
|
|
NM_145112.2:c.374T>C
|
NP_660087.1:p.Phe125Ser
|
|
|
NM_145113.2:c.*190T>C
|
NP_660088.1:n.*190T>C
|
|
|
NM_197957.3:c.171+17150T>C
|
NP_932061.1:n.171+17150T>C
|
|
|
NR_073137.1:n.525T>C
|
|
|
|
XR_429315.2:n.688T>C
|
|
|
|
NM_001320415.1:c.212T>C
|
NP_001307344.1:p.Phe71Ser
|
|
|
XM_017021312.2:c.212T>C
|
XP_016876801.1:p.Phe71Ser
|
|
|
XM_017021313.1:c.212T>C
|
XP_016876802.1:p.Phe71Ser
|
|
|
XR_001750326.2:n.746T>C
|
|
|
|
XR_001750327.2:n.665T>C
|
|
|
|
XR_002957553.1:n.1179T>C
|
|
|
|
XR_943450.3:n.769T>C
|
|
|
|
XR_943451.3:n.785T>C
|
|
|
|
XR_943452.3:n.730T>C
|
|
|
|
NM_001320415.2:c.212T>C
|
NP_001307344.1:p.Phe71Ser
|
|
|
NM_002382.5:c.401T>C
MANE Select
|
NP_002373.3:p.Phe134Ser
|
|
|
NM_145112.3:c.374T>C
|
NP_660087.1:p.Phe125Ser
|
|
|
NM_145113.3:c.*190T>C
|
NP_660088.1:n.*190T>C
|
|
|
NM_001271069.2:c.144+17150T>C
|
NP_001257998.1:n.144+17150T>C
|
|
|
NM_197957.4:c.171+17150T>C
|
NP_932061.1:n.171+17150T>C
|
|
