ENST00000683611.1:n.1102C>A
|
|
|
ENST00000265104.5:c.13769C>A
MANE Select
|
ENSP00000265104.4:p.Pro4590Gln
|
|
ENST00000681290.1:c.13724C>A
|
ENSP00000505288.1:p.Pro4575Gln
|
|
ENST00000265104.4:c.13769C>A
|
ENSP00000265104.4:p.Pro4590Gln
|
|
NM_001369.2:c.13769C>A
|
NP_001360.1:p.Pro4590Gln
|
|
XM_005248262.2:c.13724C>A
|
XP_005248319.1:p.Pro4575Gln
|
|
XM_005248262.3:c.13877C>A
|
XP_005248319.2:p.Pro4626Gln
|
|
XM_017009177.1:c.13457C>A
|
XP_016864666.1:p.Pro4486Gln
|
|
XM_017009178.1:c.12782C>A
|
XP_016864667.1:p.Pro4261Gln
|
|
XM_017009179.2:c.12782C>A
|
XP_016864668.1:p.Pro4261Gln
|
|
XM_017009185.1:c.8966C>A
|
XP_016864674.1:p.Pro2989Gln
|
|
XM_017009186.1:c.8519C>A
|
XP_016864675.1:p.Pro2840Gln
|
|
XM_017009188.1:c.7856C>A
|
XP_016864677.1:p.Pro2619Gln
|
|
XM_024454388.1:c.12782C>A
|
XP_024310156.1:p.Pro4261Gln
|
|
XM_024454389.1:c.12371C>A
|
XP_024310157.1:p.Pro4124Gln
|
|
NM_001369.3:c.13769C>A
MANE Select
|
NP_001360.1:p.Pro4590Gln
|
|