ENST00000374479.4:c.1072G>T
MANE Select
|
ENSP00000363603.3:p.Val358Phe
|
|
ENST00000374479.3:c.1072G>T
|
ENSP00000363603.3:p.Val358Phe
|
|
NM_000147.4:c.1072G>T
|
NP_000138.2:p.Val358Phe
|
|
XM_005245821.1:c.697G>T
|
XP_005245878.1:p.Val233Phe
|
|
XM_011541167.1:c.439G>T
|
XP_011539469.1:p.Val147Phe
|
|
XM_005245821.3:c.697G>T
|
XP_005245878.1:p.Val233Phe
|
|
XM_011541167.3:c.439G>T
|
XP_011539469.1:p.Val147Phe
|
|
XM_017000905.2:c.769G>T
|
XP_016856394.1:p.Val257Phe
|
|
NM_000147.5:c.1072G>T
MANE Select
|
NP_000138.2:p.Val358Phe
|
|
NR_174379.1:n.1250G>T
|
|
|
NR_174380.1:n.1299G>T
|
|
|
NR_174381.1:n.1138G>T
|
|
|
NR_174382.1:n.1535G>T
|
|
|