ENST00000265104.5:c.9722T=
MANE Select
|
ENSP00000265104.4:p.Val3241=
|
|
ENST00000681290.1:c.9677T=
|
ENSP00000505288.1:p.Val3226=
|
|
ENST00000265104.4:c.9722T=
|
ENSP00000265104.4:p.Val3241=
|
|
ENST00000504001.3:n.434T=
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|
|
NM_001369.2:c.9722T=
|
NP_001360.1:p.Val3241=
|
|
XM_005248262.2:c.9677T=
|
XP_005248319.1:p.Val3226=
|
|
XM_005248262.3:c.9830T=
|
XP_005248319.2:p.Val3277=
|
|
XM_017009177.1:c.9830T=
|
XP_016864666.1:p.Val3277=
|
|
XM_017009178.1:c.8735T=
|
XP_016864667.1:p.Val2912=
|
|
XM_017009179.2:c.8735T=
|
XP_016864668.1:p.Val2912=
|
|
XM_017009180.1:c.9830T=
|
XP_016864669.1:p.Val3277=
|
|
XM_017009181.1:c.9830T=
|
XP_016864670.1:p.Val3277=
|
|
XM_017009182.1:c.9830T=
|
XP_016864671.1:p.Val3277=
|
|
XM_017009185.1:c.4919T=
|
XP_016864674.1:p.Val1640=
|
|
XM_017009186.1:c.4472T=
|
XP_016864675.1:p.Val1491=
|
|
XM_017009188.1:c.3809T=
|
XP_016864677.1:p.Val1270=
|
|
XM_024454388.1:c.8735T=
|
XP_024310156.1:p.Val2912=
|
|
XM_024454389.1:c.8324T=
|
XP_024310157.1:p.Val2775=
|
|
NM_001369.3:c.9722T=
MANE Select
|
NP_001360.1:p.Val3241=
|
|