|
NM_133491.5:c.411G>T
(SAT2)
MANE Select
|
NP_597998.1:p.Met137Ile
|
|
ENST00000269298.10:c.411G>T
(SAT2)
MANE Select
|
ENSP00000269298.5:p.Met137Ile
|
|
NM_001289114.1:c.-61-3869C>A
(SHBG)
|
NP_001276043.1:n.-61-3869C>A
|
|
NM_001289114.2:c.-61-3869C>A
(SHBG)
|
NP_001276043.1:n.-61-3869C>A
|
|
NM_001320845.1:c.648G>T
(SAT2)
|
NP_001307774.1:p.Met216Ile
|
|
NM_001320846.1:c.546G>T
(SAT2)
|
NP_001307775.1:p.Met182Ile
|
|
NM_001320847.1:c.309G>T
(SAT2)
|
NP_001307776.1:p.Met103Ile
|
|
NM_001320847.2:c.309G>T
(SAT2)
|
NP_001307776.1:p.Met103Ile
|
|
NM_133491.3:c.411G>T
(SAT2)
|
NP_597998.1:p.Met137Ile
|
|
NM_133491.4:c.411G>T
(SAT2)
|
NP_597998.1:p.Met137Ile
|
|
ENST00000269298.9:c.411G>T
(SAT2)
|
ENSP00000269298.5:p.Met137Ile
|
|
ENST00000380466.6:n.662G>T
(SAT2)
|
|
|
ENST00000570547.5:c.-61-3869C>A
(SHBG)
|
ENSP00000458875.1:n.-61-3869C>A
|
|
ENST00000570850.5:n.539G>T
(SAT2)
|
|
|
ENST00000570914.5:n.453G>T
(SAT2)
|
|
|
ENST00000571074.5:c.*298G>T
(SAT2)
|
ENSP00000459985.1:n.*298G>T
|
|
ENST00000571195.5:n.631G>T
(SAT2)
|
|
|
ENST00000572182.5:c.-61-3869C>A
(SHBG)
|
ENSP00000458816.1:n.-61-3869C>A
|
|
ENST00000572262.5:c.-61-3869C>A
(SHBG)
|
ENSP00000459999.1:n.-61-3869C>A
|
|
ENST00000573566.1:c.309G>T
(SAT2)
|
ENSP00000458385.1:p.Met103Ile
|
|
ENST00000574539.5:c.-61-3869C>A
(SHBG)
|
ENSP00000458181.1:n.-61-3869C>A
|
|
ENST00000575314.5:c.-61-3869C>A
(SHBG)
|
ENSP00000458559.1:n.-61-3869C>A
|
|
ENST00000575826.5:c.*344G>T
(SAT2)
|
ENSP00000458818.1:n.*344G>T
|
|
ENST00000576478.5:c.-61-3869C>A
(SHBG)
|
ENSP00000461133.1:n.-61-3869C>A
|
|
ENST00000576579.5:n.224G>T
(SAT2)
|
|
|
ENST00000576686.1:n.567G>T
(SAT2)
|
|
|
ENST00000576728.5:c.-61-3869C>A
(SHBG)
|
ENSP00000459620.1:n.-61-3869C>A
|
|
ENST00000576846.1:n.1248G>T
(SAT2)
|
|
|
XM_005256432.1:c.309G>T
(SAT2)
|
XP_005256489.1:p.Met103Ile
|
|
XM_017024073.1:c.*76G>T
(SAT2)
|
XP_016879562.1:n.*76G>T
|
|
XM_017024074.1:c.*76G>T
(SAT2)
|
XP_016879563.1:n.*76G>T
|
