ENST00000683611.1:n.818G>T
|
|
|
ENST00000265104.5:c.13485G>T
MANE Select
|
ENSP00000265104.4:p.Met4495Ile
|
|
ENST00000681290.1:c.13440G>T
|
ENSP00000505288.1:p.Met4480Ile
|
|
ENST00000265104.4:c.13485G>T
|
ENSP00000265104.4:p.Met4495Ile
|
|
NM_001369.2:c.13485G>T
|
NP_001360.1:p.Met4495Ile
|
|
XM_005248262.2:c.13440G>T
|
XP_005248319.1:p.Met4480Ile
|
|
XM_005248262.3:c.13593G>T
|
XP_005248319.2:p.Met4531Ile
|
|
XM_017009177.1:c.13173G>T
|
XP_016864666.1:p.Met4391Ile
|
|
XM_017009178.1:c.12498G>T
|
XP_016864667.1:p.Met4166Ile
|
|
XM_017009179.2:c.12498G>T
|
XP_016864668.1:p.Met4166Ile
|
|
XM_017009185.1:c.8682G>T
|
XP_016864674.1:p.Met2894Ile
|
|
XM_017009186.1:c.8235G>T
|
XP_016864675.1:p.Met2745Ile
|
|
XM_017009188.1:c.7572G>T
|
XP_016864677.1:p.Met2524Ile
|
|
XM_024454388.1:c.12498G>T
|
XP_024310156.1:p.Met4166Ile
|
|
XM_024454389.1:c.12087G>T
|
XP_024310157.1:p.Met4029Ile
|
|
NM_001369.3:c.13485G>T
MANE Select
|
NP_001360.1:p.Met4495Ile
|
|