|
ENST00000400017.7:c.1922C>G
MANE Select
|
ENSP00000382895.2:p.Ala641Gly
|
|
|
ENST00000382933.8:c.688+2773C>G
|
ENSP00000372391.4:n.688+2773C>G
|
|
|
ENST00000400017.6:c.1922C>G
|
ENSP00000382895.2:p.Ala641Gly
|
|
|
ENST00000553500.5:n.328+52C>G
|
|
|
|
ENST00000553927.1:n.854C>G
|
|
|
|
ENST00000554303.1:c.308C>G
|
ENSP00000450426.1:p.Ala103Gly
|
|
|
ENST00000555322.5:c.349C>G
|
|
|
|
ENST00000555489.5:c.212+52C>G
|
ENSP00000451044.1:n.212+52C>G
|
|
|
ENST00000555587.5:c.347C>G
|
ENSP00000451262.1:p.Ala116Gly
|
|
|
ENST00000556336.5:c.1681+2773C>G
|
ENSP00000450445.1:n.1681+2773C>G
|
|
|
ENST00000557771.5:c.1808C>G
|
ENSP00000451219.1:p.Ala603Gly
|
|
|
NM_020366.3:c.1922C>G
|
NP_065099.3:p.Ala641Gly
|
|
|
XM_005267879.2:c.848C>G
|
XP_005267936.1:p.Ala283Gly
|
|
|
XM_005267880.2:c.815C>G
|
XP_005267937.1:p.Ala272Gly
|
|
|
XM_005267881.2:c.296C>G
|
XP_005267938.1:p.Ala99Gly
|
|
|
XM_011536978.1:c.848C>G
|
XP_011535280.1:p.Ala283Gly
|
|
|
XM_011536979.1:c.796+52C>G
|
XP_011535281.1:n.796+52C>G
|
|
|
XM_011536980.1:c.796+52C>G
|
XP_011535282.1:n.796+52C>G
|
|
|
XM_011536981.1:c.848C>G
|
XP_011535283.1:p.Ala283Gly
|
|
|
XM_011536982.1:c.796+52C>G
|
XP_011535284.1:n.796+52C>G
|
|
|
XM_011536983.1:c.1889C>G
|
XP_011535285.1:p.Ala630Gly
|
|
|
XM_005267881.3:c.296C>G
|
XP_005267938.1:p.Ala99Gly
|
|
|
XM_017021473.1:c.848C>G
|
XP_016876962.1:p.Ala283Gly
|
|
|
XM_024449663.1:c.848C>G
|
XP_024305431.1:p.Ala283Gly
|
|
|
XM_024449664.1:c.848C>G
|
XP_024305432.1:p.Ala283Gly
|
|
|
XM_024449665.1:c.796+52C>G
|
XP_024305433.1:n.796+52C>G
|
|
|
XM_024449666.1:c.796+52C>G
|
XP_024305434.1:n.796+52C>G
|
|
|
NM_001377523.1:c.688+2773C>G
|
NP_001364452.1:n.688+2773C>G
|
|
|
NM_001377948.1:c.848C>G
|
NP_001364877.1:p.Ala283Gly
|
|
|
NM_001377949.1:c.796+52C>G
|
NP_001364878.1:n.796+52C>G
|
|
|
NM_001377950.1:c.688+2773C>G
|
NP_001364879.1:n.688+2773C>G
|
|
|
NM_001377951.1:c.190+2773C>G
|
NP_001364880.1:n.190+2773C>G
|
|
|
NM_020366.4:c.1922C>G
MANE Select
|
NP_065099.3:p.Ala641Gly
|
|
