ENST00000704337.1:n.373G>T
|
|
|
ENST00000378536.5:c.1205G>T
MANE Select
|
ENSP00000367797.4:p.Arg402Leu
|
|
ENST00000378536.4:c.1205G>T
|
ENSP00000367797.4:p.Arg402Leu
|
|
NM_003036.3:c.1205G>T
|
NP_003027.1:p.Arg402Leu
|
|
XM_005244775.2:c.1205G>T
|
XP_005244832.1:p.Arg402Leu
|
|
XM_005244776.3:c.335G>T
|
XP_005244833.1:p.Arg112Leu
|
|
XM_005244775.3:c.1205G>T
|
XP_005244832.1:p.Arg402Leu
|
|
XM_005244776.4:c.335G>T
|
XP_005244833.1:p.Arg112Leu
|
|
XM_017002128.1:c.713G>T
|
XP_016857617.1:p.Arg238Leu
|
|
NM_003036.4:c.1205G>T
MANE Select
|
NP_003027.1:p.Arg402Leu
|
|