ENST00000262367.10:c.7074T>C
MANE Select
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ENSP00000262367.5:p.Pro2358=
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ENST00000262367.9:c.7074T>C
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ENSP00000262367.5:p.Pro2358=
|
|
ENST00000382070.7:c.6960T>C
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ENSP00000371502.3:p.Pro2320=
|
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NM_001079846.1:c.6960T>C
|
NP_001073315.1:p.Pro2320=
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|
NM_004380.2:c.7074T>C
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NP_004371.2:p.Pro2358=
|
|
XM_005255124.3:c.7029T>C
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XP_005255181.1:p.Pro2343=
|
|
XM_005255125.3:c.6657T>C
|
XP_005255182.1:p.Pro2219=
|
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XM_006720848.2:c.6813T>C
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XP_006720911.1:p.Pro2271=
|
|
XM_011522380.1:c.7020T>C
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XP_011520682.1:p.Pro2340=
|
|
XM_011522381.1:c.6321T>C
|
XP_011520683.1:p.Pro2107=
|
|
XM_005255124.4:c.7029T>C
|
XP_005255181.1:p.Pro2343=
|
|
XM_005255125.4:c.6657T>C
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XP_005255182.1:p.Pro2219=
|
|
XM_006720848.3:c.6813T>C
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XP_006720911.1:p.Pro2271=
|
|
XM_011522381.2:c.6321T>C
|
XP_011520683.1:p.Pro2107=
|
|
XM_017022944.1:c.7068T>C
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XP_016878433.1:p.Pro2356=
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|
NM_004380.3:c.7074T>C
MANE Select
|
NP_004371.2:p.Pro2358=
|
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