ENST00000645828.1:n.2717G>T
|
|
|
ENST00000651671.1:c.4910G>T
MANE Select
|
ENSP00000498587.1:p.Gly1637Val
|
|
ENST00000679595.1:c.4910G>T
|
ENSP00000506241.1:p.Gly1637Val
|
|
ENST00000680133.1:c.4796G>T
|
ENSP00000505319.1:p.Gly1599Val
|
|
ENST00000680218.1:c.4790G>T
|
ENSP00000505339.1:p.Gly1597Val
|
|
ENST00000680668.1:c.4796G>T
|
ENSP00000506336.1:p.Gly1599Val
|
|
ENST00000680778.1:c.2507G>T
|
ENSP00000506033.1:p.Gly836Val
|
|
ENST00000680924.1:c.*2310G>T
|
ENSP00000506031.1:n.*2310G>T
|
|
ENST00000681135.1:c.*2519G>T
|
ENSP00000506636.1:n.*2519G>T
|
|
ENST00000681298.1:n.1723G>T
|
|
|
ENST00000681454.1:c.*4146G>T
|
ENSP00000505763.1:n.*4146G>T
|
|
ENST00000277541.6:c.4910G>T
|
ENSP00000277541.6:p.Gly1637Val
|
|
ENST00000494783.1:n.65G>T
|
|
|
NM_017617.3:c.4910G>T
|
NP_060087.3:p.Gly1637Val
|
|
XM_011518717.1:c.4211G>T
|
XP_011517019.1:p.Gly1404Val
|
|
NM_017617.5:c.4910G>T
MANE Select
|
NP_060087.3:p.Gly1637Val
|
|
XM_011518717.2:c.4187G>T
|
XP_011517019.2:p.Gly1396Val
|
|