ENST00000683611.1:n.1101C>T
|
|
|
ENST00000265104.5:c.13768C>T
MANE Select
|
ENSP00000265104.4:p.Pro4590Ser
|
|
ENST00000681290.1:c.13723C>T
|
ENSP00000505288.1:p.Pro4575Ser
|
|
ENST00000265104.4:c.13768C>T
|
ENSP00000265104.4:p.Pro4590Ser
|
|
NM_001369.2:c.13768C>T
|
NP_001360.1:p.Pro4590Ser
|
|
XM_005248262.2:c.13723C>T
|
XP_005248319.1:p.Pro4575Ser
|
|
XM_005248262.3:c.13876C>T
|
XP_005248319.2:p.Pro4626Ser
|
|
XM_017009177.1:c.13456C>T
|
XP_016864666.1:p.Pro4486Ser
|
|
XM_017009178.1:c.12781C>T
|
XP_016864667.1:p.Pro4261Ser
|
|
XM_017009179.2:c.12781C>T
|
XP_016864668.1:p.Pro4261Ser
|
|
XM_017009185.1:c.8965C>T
|
XP_016864674.1:p.Pro2989Ser
|
|
XM_017009186.1:c.8518C>T
|
XP_016864675.1:p.Pro2840Ser
|
|
XM_017009188.1:c.7855C>T
|
XP_016864677.1:p.Pro2619Ser
|
|
XM_024454388.1:c.12781C>T
|
XP_024310156.1:p.Pro4261Ser
|
|
XM_024454389.1:c.12370C>T
|
XP_024310157.1:p.Pro4124Ser
|
|
NM_001369.3:c.13768C>T
MANE Select
|
NP_001360.1:p.Pro4590Ser
|
|