ENST00000470094.2:c.485G>C
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ENSP00000434898.2:p.Gly162Ala
|
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ENST00000528762.2:c.485G>C
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ENSP00000433168.2:p.Gly162Ala
|
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ENST00000530893.7:c.116G>C
|
ENSP00000499438.2:p.Gly39Ala
|
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ENST00000665585.2:c.485G>C
|
ENSP00000499570.2:p.Gly162Ala
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ENST00000666593.2:c.485G>C
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ENSP00000499256.2:p.Gly162Ala
|
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ENST00000700202.2:c.485G>C
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ENSP00000514856.2:p.Gly162Ala
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ENST00000700200.1:n.356G>C
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ENST00000700201.1:c.*264G>C
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ENSP00000514855.1:n.*264G>C
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ENST00000380152.8:c.485G>C
MANE Select
|
ENSP00000369497.3:p.Gly162Ala
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ENST00000544455.6:c.485G>C
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ENSP00000439902.1:p.Gly162Ala
|
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ENST00000614259.2:c.485G>C
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ENSP00000506251.1:p.Gly162Ala
|
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ENST00000680887.1:c.485G>C
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ENSP00000505508.1:p.Gly162Ala
|
|
ENST00000380152.7:c.485G>C
|
ENSP00000369497.3:p.Gly162Ala
|
|
ENST00000530893.6:n.683G>C
|
|
|
ENST00000544455.5:c.485G>C
|
ENSP00000439902.1:p.Gly162Ala
|
|
ENST00000614259.1:n.485G>C
|
|
|
NM_000059.3:c.485G>C , LRG_293t1:c.485G>C
|
NP_000050.2:p.Gly162Ala
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XM_011535203.1:c.485G>C
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XP_011533505.1:p.Gly162Ala
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XM_011535204.1:c.485G>C
|
XP_011533506.1:p.Gly162Ala
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XM_011535205.1:c.485G>C
|
XP_011533507.1:p.Gly162Ala
|
|
NM_000059.4:c.485G>C
MANE Select
|
NP_000050.3:p.Gly162Ala
|
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