ENST00000294304.12:c.3953A>C
MANE Select
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ENSP00000294304.6:p.Asp1318Ala
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ENST00000294304.11:c.3953A>C
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ENSP00000294304.6:p.Asp1318Ala
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|
ENST00000529993.5:c.*2559A>C
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ENSP00000436652.1:n.*2559A>C
|
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NM_001291902.1:c.2210A>C
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NP_001278831.1:p.Asp737Ala
|
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NM_002335.3:c.3953A>C
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NP_002326.2:p.Asp1318Ala
|
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XM_005273994.2:c.3953A>C
|
XP_005274051.1:p.Asp1318Ala
|
|
XM_011545029.1:c.3980A>C
|
XP_011543331.1:p.Asp1327Ala
|
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XM_011545030.1:c.3980A>C
|
XP_011543332.1:p.Asp1327Ala
|
|
XM_011545031.1:c.3980A>C
|
XP_011543333.1:p.Asp1327Ala
|
|
XR_949925.1:n.3995A>C
|
|
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XR_949926.1:n.3995A>C
|
|
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XM_017017735.1:c.2210A>C
|
XP_016873224.1:p.Asp737Ala
|
|
XM_017017736.1:c.1493A>C
|
XP_016873225.1:p.Asp498Ala
|
|
XR_949925.2:n.3995A>C
|
|
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XR_949926.2:n.3995A>C
|
|
|
NM_002335.4:c.3953A>C
MANE Select
|
NP_002326.2:p.Asp1318Ala
|
|
NM_001291902.2:c.2210A>C
|
NP_001278831.1:p.Asp737Ala
|
|