ENST00000683611.1:n.1116T>C
|
|
|
ENST00000265104.5:c.13783T>C
MANE Select
|
ENSP00000265104.4:p.Leu4595=
|
|
ENST00000681290.1:c.13738T>C
|
ENSP00000505288.1:p.Leu4580=
|
|
ENST00000265104.4:c.13783T>C
|
ENSP00000265104.4:p.Leu4595=
|
|
NM_001369.2:c.13783T>C
|
NP_001360.1:p.Leu4595=
|
|
XM_005248262.2:c.13738T>C
|
XP_005248319.1:p.Leu4580=
|
|
XM_005248262.3:c.13891T>C
|
XP_005248319.2:p.Leu4631=
|
|
XM_017009177.1:c.13471T>C
|
XP_016864666.1:p.Leu4491=
|
|
XM_017009178.1:c.12796T>C
|
XP_016864667.1:p.Leu4266=
|
|
XM_017009179.2:c.12796T>C
|
XP_016864668.1:p.Leu4266=
|
|
XM_017009185.1:c.8980T>C
|
XP_016864674.1:p.Leu2994=
|
|
XM_017009186.1:c.8533T>C
|
XP_016864675.1:p.Leu2845=
|
|
XM_017009188.1:c.7870T>C
|
XP_016864677.1:p.Leu2624=
|
|
XM_024454388.1:c.12796T>C
|
XP_024310156.1:p.Leu4266=
|
|
XM_024454389.1:c.12385T>C
|
XP_024310157.1:p.Leu4129=
|
|
NM_001369.3:c.13783T>C
MANE Select
|
NP_001360.1:p.Leu4595=
|
|