ENST00000683611.1:n.1103A>T
|
|
|
ENST00000265104.5:c.13770A>T
MANE Select
|
ENSP00000265104.4:p.Pro4590=
|
|
ENST00000681290.1:c.13725A>T
|
ENSP00000505288.1:p.Pro4575=
|
|
ENST00000265104.4:c.13770A>T
|
ENSP00000265104.4:p.Pro4590=
|
|
NM_001369.2:c.13770A>T
|
NP_001360.1:p.Pro4590=
|
|
XM_005248262.2:c.13725A>T
|
XP_005248319.1:p.Pro4575=
|
|
XM_005248262.3:c.13878A>T
|
XP_005248319.2:p.Pro4626=
|
|
XM_017009177.1:c.13458A>T
|
XP_016864666.1:p.Pro4486=
|
|
XM_017009178.1:c.12783A>T
|
XP_016864667.1:p.Pro4261=
|
|
XM_017009179.2:c.12783A>T
|
XP_016864668.1:p.Pro4261=
|
|
XM_017009185.1:c.8967A>T
|
XP_016864674.1:p.Pro2989=
|
|
XM_017009186.1:c.8520A>T
|
XP_016864675.1:p.Pro2840=
|
|
XM_017009188.1:c.7857A>T
|
XP_016864677.1:p.Pro2619=
|
|
XM_024454388.1:c.12783A>T
|
XP_024310156.1:p.Pro4261=
|
|
XM_024454389.1:c.12372A>T
|
XP_024310157.1:p.Pro4124=
|
|
NM_001369.3:c.13770A>T
MANE Select
|
NP_001360.1:p.Pro4590=
|
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