ENST00000261769.10:c.1870T=
MANE Select
|
ENSP00000261769.4:p.Ser624=
|
|
ENST00000261769.9:c.1870T=
|
ENSP00000261769.4:p.Ser624=
|
|
ENST00000422392.6:c.1687T=
|
ENSP00000414946.2:p.Ser563=
|
|
ENST00000562836.5:n.1941T=
|
|
|
ENST00000566510.5:c.*536T=
|
ENSP00000458139.1:n.*536T=
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|
ENST00000566612.5:c.*110T=
|
ENSP00000454782.1:n.*110T=
|
|
ENST00000611625.4:c.1933T=
|
ENSP00000481063.1:p.Ser645=
|
|
ENST00000612417.4:c.1830+40T=
|
ENSP00000478360.1:n.1830+40T=
|
|
ENST00000621016.4:c.1865+5T=
|
ENSP00000480664.1:n.1865+5T=
|
|
NM_004360.3:c.1870T= , LRG_301t1:c.1870T=
|
NP_004351.1:p.Ser624=
|
|
XM_011523488.1:c.1135T=
|
XP_011521790.1:p.Ser379=
|
|
XM_011523489.1:c.1135T=
|
XP_011521791.1:p.Ser379=
|
|
NM_001317184.1:c.1687T=
|
NP_001304113.1:p.Ser563=
|
|
NM_001317185.1:c.322T=
|
NP_001304114.1:p.Ser108=
|
|
NM_001317186.1:c.-96T=
|
NP_001304115.1:n.-96T=
|
|
NM_004360.4:c.1870T=
|
NP_004351.1:p.Ser624=
|
|
NM_004360.5:c.1870T=
MANE Select
|
NP_004351.1:p.Ser624=
|
|
NM_001317184.2:c.1687T=
|
NP_001304113.1:p.Ser563=
|
|
NM_001317185.2:c.322T=
|
NP_001304114.1:p.Ser108=
|
|
NM_001317186.2:c.-96T=
|
NP_001304115.1:n.-96T=
|
|