ENST00000262367.10:c.6939C>T
MANE Select
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ENSP00000262367.5:p.Pro2313=
|
|
ENST00000262367.9:c.6939C>T
|
ENSP00000262367.5:p.Pro2313=
|
|
ENST00000382070.7:c.6825C>T
|
ENSP00000371502.3:p.Pro2275=
|
|
NM_001079846.1:c.6825C>T
|
NP_001073315.1:p.Pro2275=
|
|
NM_004380.2:c.6939C>T
|
NP_004371.2:p.Pro2313=
|
|
XM_005255124.3:c.6894C>T
|
XP_005255181.1:p.Pro2298=
|
|
XM_005255125.3:c.6522C>T
|
XP_005255182.1:p.Pro2174=
|
|
XM_006720848.2:c.6678C>T
|
XP_006720911.1:p.Pro2226=
|
|
XM_011522380.1:c.6885C>T
|
XP_011520682.1:p.Pro2295=
|
|
XM_011522381.1:c.6186C>T
|
XP_011520683.1:p.Pro2062=
|
|
XM_005255124.4:c.6894C>T
|
XP_005255181.1:p.Pro2298=
|
|
XM_005255125.4:c.6522C>T
|
XP_005255182.1:p.Pro2174=
|
|
XM_006720848.3:c.6678C>T
|
XP_006720911.1:p.Pro2226=
|
|
XM_011522381.2:c.6186C>T
|
XP_011520683.1:p.Pro2062=
|
|
XM_017022944.1:c.6933C>T
|
XP_016878433.1:p.Pro2311=
|
|
NM_004380.3:c.6939C>T
MANE Select
|
NP_004371.2:p.Pro2313=
|
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