ENST00000683611.1:n.1189T>A
|
|
|
ENST00000265104.5:c.13856T>A
MANE Select
|
ENSP00000265104.4:p.Leu4619His
|
|
ENST00000681290.1:c.13811T>A
|
ENSP00000505288.1:p.Leu4604His
|
|
ENST00000265104.4:c.13856T>A
|
ENSP00000265104.4:p.Leu4619His
|
|
NM_001369.2:c.13856T>A
|
NP_001360.1:p.Leu4619His
|
|
XM_005248262.2:c.13811T>A
|
XP_005248319.1:p.Leu4604His
|
|
XM_005248262.3:c.13964T>A
|
XP_005248319.2:p.Leu4655His
|
|
XM_017009177.1:c.13544T>A
|
XP_016864666.1:p.Leu4515His
|
|
XM_017009178.1:c.12869T>A
|
XP_016864667.1:p.Leu4290His
|
|
XM_017009179.2:c.12869T>A
|
XP_016864668.1:p.Leu4290His
|
|
XM_017009185.1:c.9053T>A
|
XP_016864674.1:p.Leu3018His
|
|
XM_017009186.1:c.8606T>A
|
XP_016864675.1:p.Leu2869His
|
|
XM_017009188.1:c.7943T>A
|
XP_016864677.1:p.Leu2648His
|
|
XM_024454388.1:c.12869T>A
|
XP_024310156.1:p.Leu4290His
|
|
XM_024454389.1:c.12458T>A
|
XP_024310157.1:p.Leu4153His
|
|
NM_001369.3:c.13856T>A
MANE Select
|
NP_001360.1:p.Leu4619His
|
|