ENST00000225573.5:c.625G>C
|
ENSP00000225573.5:p.Glu209Gln
|
|
ENST00000434554.7:c.700G>C
|
ENSP00000399960.3:p.Glu234Gln
|
|
ENST00000582171.6:c.*419G>C
|
ENSP00000463994.1:n.*419G>C
|
|
ENST00000584061.6:c.685G>C
|
ENSP00000463972.2:p.Glu229Gln
|
|
ENST00000584806.2:n.423G>C
|
|
|
ENST00000641305.1:n.2253G>C
|
|
|
ENST00000641323.1:c.*773G>C
|
ENSP00000492965.1:n.*773G>C
|
|
ENST00000641427.1:n.754G>C
|
|
|
ENST00000641703.1:c.470G>C
|
ENSP00000493219.1:n.470G>C
|
|
ENST00000641709.1:c.*576G>C
|
ENSP00000493349.1:n.*576G>C
|
|
ENST00000641856.1:c.*1262G>C
|
ENSP00000493224.1:n.*1262G>C
|
|
ENST00000642017.2:c.754G>C
MANE Select
|
ENSP00000493302.2:p.Glu252Gln
|
|
ENST00000225573.4:c.754G>C
|
ENSP00000225573.4:p.Glu252Gln
|
|
ENST00000434554.6:c.625G>C
|
ENSP00000399960.2:p.Glu209Gln
|
|
ENST00000582171.5:c.*419G>C
|
ENSP00000463994.1:n.*419G>C
|
|
ENST00000584806.1:n.423G>C
|
|
|
NM_018129.3:c.754G>C
|
NP_060599.1:p.Glu252Gln
|
|
XM_005257500.2:c.514G>C
|
XP_005257557.1:p.Glu172Gln
|
|
XM_011524968.1:c.469G>C
|
XP_011523270.1:p.Glu157Gln
|
|
XM_005257500.3:c.514G>C
|
XP_005257557.1:p.Glu172Gln
|
|
XM_011524968.2:c.469G>C
|
XP_011523270.1:p.Glu157Gln
|
|
XM_017024813.1:c.514G>C
|
XP_016880302.1:p.Glu172Gln
|
|
NM_018129.4:c.754G>C
MANE Select
|
NP_060599.1:p.Glu252Gln
|
|