ENST00000298910.12:c.7104A>G
MANE Select
|
ENSP00000298910.7:p.Gln2368=
|
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ENST00000636518.1:c.901A>G
|
|
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ENST00000679360.1:c.*6013A>G
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ENSP00000505368.1:n.*6013A>G
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ENST00000679532.1:c.2878A>G
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|
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ENST00000679683.1:c.894A>G
|
|
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ENST00000680018.1:c.2549A>G
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ENSP00000505347.1:n.2549A>G
|
|
ENST00000680422.1:c.4191A>G
|
|
|
ENST00000680425.1:c.2271A>G
|
ENSP00000506459.1:n.2271A>G
|
|
ENST00000680453.1:c.2561A>G
|
|
|
ENST00000680790.1:c.6849A>G
|
ENSP00000505335.1:p.Gln2283=
|
|
ENST00000681136.1:n.3088A>G
|
|
|
ENST00000681696.1:c.2787A>G
|
ENSP00000505871.1:p.Gln929=
|
|
ENST00000681773.1:n.311A>G
|
|
|
ENST00000298910.11:c.7104A>G
|
ENSP00000298910.7:p.Gln2368=
|
|
ENST00000430804.5:c.4400A>G
|
|
|
ENST00000479187.5:n.3785A>G
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|
|
NM_198578.3:c.7104A>G
|
NP_940980.3:p.Gln2368=
|
|
XM_005268629.2:c.7104A>G
|
XP_005268686.1:p.Gln2368=
|
|
XM_011537877.1:c.7104A>G
|
XP_011536179.1:p.Gln2368=
|
|
XM_011537879.1:c.5901A>G
|
XP_011536181.1:p.Gln1967=
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XR_944868.1:n.485-8650T>C
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|
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XM_005268629.4:c.7104A>G
|
XP_005268686.1:p.Gln2368=
|
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XM_011537877.3:c.7104A>G
|
XP_011536179.1:p.Gln2368=
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|
XM_017018787.1:c.4020A>G
|
XP_016874276.1:p.Gln1340=
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XM_017018788.2:c.3366A>G
|
XP_016874277.1:p.Gln1122=
|
|
XM_024448833.1:c.5901A>G
|
XP_024304601.1:p.Gln1967=
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XR_944868.2:n.485-8650T>C
|
|
|
NM_198578.4:c.7104A>G
MANE Select
|
NP_940980.4:p.Gln2368=
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