ENST00000288840.10:c.963G>T
MANE Select
|
ENSP00000288840.5:p.Met321Ile
|
|
ENST00000288840.9:c.963G>T
|
ENSP00000288840.5:p.Met321Ile
|
|
ENST00000557916.5:c.1095G>T
|
ENSP00000452955.1:n.1095G>T
|
|
ENST00000559931.5:c.267G>T
|
ENSP00000453446.1:n.267G>T
|
|
NM_005585.4:c.963G>T
|
NP_005576.3:p.Met321Ile
|
|
NR_027654.1:n.2018G>T
|
|
|
XM_011521561.1:c.180G>T
|
XP_011519863.1:p.Met60Ile
|
|
XR_931825.1:n.2362G>T
|
|
|
XM_011521561.2:c.180G>T
|
XP_011519863.1:p.Met60Ile
|
|
NM_005585.5:c.963G>T
MANE Select
|
NP_005576.3:p.Met321Ile
|
|
NR_027654.2:n.2118G>T
|
|
|