ENST00000698234.1:n.1529G>C
|
|
|
ENST00000698317.1:n.2145G>C
|
|
|
ENST00000698318.1:n.1928G>C
|
|
|
ENST00000698319.1:n.1291G>C
|
|
|
ENST00000698320.1:n.1179G>C
|
|
|
ENST00000470127.2:n.1192G>C
|
|
|
ENST00000475699.6:c.683G>C
|
ENSP00000419854.3:p.Gly228Ala
|
|
ENST00000483674.3:n.601G>C
|
|
|
ENST00000601016.6:c.719G>C
MANE Select
|
ENSP00000469981.1:p.Gly240Ala
|
|
ENST00000612012.5:c.677G>C
|
ENSP00000482070.2:p.Gly226Ala
|
|
ENST00000612460.5:c.629G>C
|
ENSP00000481037.1:p.Gly210Ala
|
|
ENST00000614595.2:n.2066G>C
|
|
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ENST00000615658.5:n.1308G>C
|
|
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ENST00000616020.5:c.731G>C
|
ENSP00000483636.2:p.Gly244Ala
|
|
ENST00000617701.5:c.*732G>C
|
ENSP00000481645.1:n.*732G>C
|
|
ENST00000651139.1:c.-65G>C
|
ENSP00000498957.1:n.-65G>C
|
|
ENST00000652354.1:c.401G>C
|
ENSP00000498734.1:p.Gly134Ala
|
|
ENST00000652358.1:c.512G>C
|
ENSP00000498464.1:p.Gly171Ala
|
|
ENST00000652390.1:c.638G>C
|
ENSP00000498858.1:p.Gly213Ala
|
|
ENST00000652476.1:n.1385G>C
|
|
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ENST00000652644.1:c.332G>C
|
ENSP00000498496.1:p.Gly111Ala
|
|
ENST00000652682.1:c.776G>C
|
ENSP00000498288.1:p.Gly259Ala
|
|
ENST00000652685.1:n.1072G>C
|
|
|
ENST00000369776.8:c.629G>C
|
ENSP00000358791.4:p.Gly210Ala
|
|
ENST00000426231.5:c.716G>C
|
|
|
ENST00000475699.5:c.677G>C
|
ENSP00000419854.2:p.Gly226Ala
|
|
ENST00000494912.5:n.1408G>C
|
|
|
ENST00000498029.1:n.177G>C
|
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ENST00000601016.5:c.719G>C
|
ENSP00000469981.1:p.Gly240Ala
|
|
ENST00000612460.4:c.629G>C
|
ENSP00000481037.1:p.Gly210Ala
|
|
ENST00000613002.4:c.587G>C
|
ENSP00000478154.1:p.Gly196Ala
|
|
ENST00000615986.4:c.*447G>C
|
ENSP00000480133.1:n.*447G>C
|
|
NM_000116.4:c.719G>C
|
NP_000107.1:p.Gly240Ala
|
|
NM_001303465.1:c.731G>C
|
NP_001290394.1:p.Gly244Ala
|
|
NM_181311.3:c.629G>C
|
NP_851828.1:p.Gly210Ala
|
|
NM_181312.3:c.677G>C
|
NP_851829.1:p.Gly226Ala
|
|
NM_181313.3:c.587G>C
|
NP_851830.1:p.Gly196Ala
|
|
NR_024048.2:n.1061G>C
|
|
|
XM_006724836.1:c.773G>C
|
XP_006724899.1:p.Gly258Ala
|
|
XM_006724837.1:c.758G>C
|
XP_006724900.1:p.Gly253Ala
|
|
XM_006724839.1:c.641G>C
|
XP_006724902.1:p.Gly214Ala
|
|
XM_006724841.2:c.512G>C
|
XP_006724904.1:p.Gly171Ala
|
|
XM_006724842.2:c.422G>C
|
XP_006724905.1:p.Gly141Ala
|
|
XM_011531189.1:c.560G>C
|
XP_011529491.1:p.Gly187Ala
|
|
XM_011531190.1:c.512G>C
|
XP_011529492.1:p.Gly171Ala
|
|
XM_011531191.1:c.443G>C
|
XP_011529493.1:p.Gly148Ala
|
|
XM_011531192.1:c.440G>C
|
XP_011529494.1:p.Gly147Ala
|
|
XR_938511.1:n.1067G>C
|
|
|
XM_006724841.4:c.512G>C
|
XP_006724904.1:p.Gly171Ala
|
|
XM_006724842.4:c.422G>C
|
XP_006724905.1:p.Gly141Ala
|
|
XM_011531191.2:c.443G>C
|
XP_011529493.1:p.Gly148Ala
|
|
XM_017029761.1:c.704G>C
|
XP_016885250.1:p.Gly235Ala
|
|
XM_017029762.1:c.683G>C
|
XP_016885251.1:p.Gly228Ala
|
|
XM_017029763.1:c.506G>C
|
XP_016885252.1:p.Gly169Ala
|
|
XM_017029764.1:c.440G>C
|
XP_016885253.1:p.Gly147Ala
|
|
XM_017029765.2:c.380G>C
|
XP_016885254.1:p.Gly127Ala
|
|
XM_024452431.1:c.677G>C
|
XP_024308199.1:p.Gly226Ala
|
|
NM_000116.5:c.719G>C
MANE Select
|
NP_000107.1:p.Gly240Ala
|
|
NM_001303465.2:c.731G>C
|
NP_001290394.1:p.Gly244Ala
|
|
NM_181311.4:c.629G>C
|
NP_851828.1:p.Gly210Ala
|
|
NM_181312.4:c.677G>C
|
NP_851829.1:p.Gly226Ala
|
|
NM_181313.4:c.587G>C
|
NP_851830.1:p.Gly196Ala
|
|
NR_024048.3:n.1040G>C
|
|
|