ENST00000265104.5:c.11499G>T
MANE Select
|
ENSP00000265104.4:p.Met3833Ile
|
|
ENST00000681290.1:c.11454G>T
|
ENSP00000505288.1:p.Met3818Ile
|
|
ENST00000265104.4:c.11499G>T
|
ENSP00000265104.4:p.Met3833Ile
|
|
NM_001369.2:c.11499G>T
|
NP_001360.1:p.Met3833Ile
|
|
XM_005248262.2:c.11454G>T
|
XP_005248319.1:p.Met3818Ile
|
|
XM_005248262.3:c.11607G>T
|
XP_005248319.2:p.Met3869Ile
|
|
XM_017009177.1:c.11607G>T
|
XP_016864666.1:p.Met3869Ile
|
|
XM_017009178.1:c.10512G>T
|
XP_016864667.1:p.Met3504Ile
|
|
XM_017009179.2:c.10512G>T
|
XP_016864668.1:p.Met3504Ile
|
|
XM_017009180.1:c.11607G>T
|
XP_016864669.1:p.Met3869Ile
|
|
XM_017009181.1:c.11607G>T
|
XP_016864670.1:p.Met3869Ile
|
|
XM_017009182.1:c.11363G>T
|
XP_016864671.1:p.Cys3788Phe
|
|
XM_017009185.1:c.6696G>T
|
XP_016864674.1:p.Met2232Ile
|
|
XM_017009186.1:c.6249G>T
|
XP_016864675.1:p.Met2083Ile
|
|
XM_017009188.1:c.5586G>T
|
XP_016864677.1:p.Met1862Ile
|
|
XM_024454388.1:c.10512G>T
|
XP_024310156.1:p.Met3504Ile
|
|
XM_024454389.1:c.10101G>T
|
XP_024310157.1:p.Met3367Ile
|
|
NM_001369.3:c.11499G>T
MANE Select
|
NP_001360.1:p.Met3833Ile
|
|