ENST00000298910.12:c.6469G>C
MANE Select
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ENSP00000298910.7:p.Ala2157Pro
|
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ENST00000636518.1:c.266G>C
|
|
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ENST00000679360.1:c.*5378G>C
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ENSP00000505368.1:n.*5378G>C
|
|
ENST00000679532.1:c.2243G>C
|
|
|
ENST00000679683.1:c.259G>C
|
|
|
ENST00000680018.1:c.1914G>C
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ENSP00000505347.1:n.1914G>C
|
|
ENST00000680422.1:c.2114G>C
|
|
|
ENST00000680425.1:c.1636G>C
|
ENSP00000506459.1:n.1636G>C
|
|
ENST00000680453.1:c.1926G>C
|
|
|
ENST00000680790.1:c.6214G>C
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ENSP00000505335.1:p.Ala2072Pro
|
|
ENST00000681136.1:n.2453G>C
|
|
|
ENST00000681696.1:c.2152G>C
|
ENSP00000505871.1:p.Ala718Pro
|
|
ENST00000298910.11:c.6469G>C
|
ENSP00000298910.7:p.Ala2157Pro
|
|
ENST00000430804.5:c.3765G>C
|
|
|
ENST00000479187.5:n.3150G>C
|
|
|
NM_198578.3:c.6469G>C
|
NP_940980.3:p.Ala2157Pro
|
|
XM_005268629.2:c.6469G>C
|
XP_005268686.1:p.Ala2157Pro
|
|
XM_011537877.1:c.6469G>C
|
XP_011536179.1:p.Ala2157Pro
|
|
XM_011537878.1:c.6469G>C
|
XP_011536180.1:p.Ala2157Pro
|
|
XM_011537879.1:c.5266G>C
|
XP_011536181.1:p.Ala1756Pro
|
|
XM_005268629.4:c.6469G>C
|
XP_005268686.1:p.Ala2157Pro
|
|
XM_011537877.3:c.6469G>C
|
XP_011536179.1:p.Ala2157Pro
|
|
XM_017018787.1:c.3385G>C
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XP_016874276.1:p.Ala1129Pro
|
|
XM_017018788.2:c.2731G>C
|
XP_016874277.1:p.Ala911Pro
|
|
XM_024448833.1:c.5266G>C
|
XP_024304601.1:p.Ala1756Pro
|
|
NM_198578.4:c.6469G>C
MANE Select
|
NP_940980.4:p.Ala2157Pro
|
|