ENST00000399503.4:c.828A>C
MANE Select
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ENSP00000382423.3:p.Pro276=
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|
ENST00000399503.3:c.828A>C
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ENSP00000382423.3:p.Pro276=
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|
NM_005921.1:c.828A>C
|
NP_005912.1:p.Pro276=
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XM_005248519.3:c.450A>C
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XP_005248576.2:p.Pro150=
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|
XM_011543406.1:c.573A>C
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XP_011541708.1:p.Pro191=
|
|
XM_011543407.1:c.828A>C
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XP_011541709.1:p.Pro276=
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XM_011543408.1:c.828A>C
|
XP_011541710.1:p.Pro276=
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|
XM_017009484.1:c.417A>C
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XP_016864973.1:p.Pro139=
|
|
XM_017009485.1:c.339A>C
|
XP_016864974.1:p.Pro113=
|
|
XR_001742068.2:n.859A>C
|
|
|
NM_005921.2:c.828A>C
MANE Select
|
NP_005912.1:p.Pro276=
|
|