ENST00000281928.9:c.2737T>C
MANE Select
|
ENSP00000281928.3:p.Phe913Leu
|
|
ENST00000548743.2:c.2707T>C
|
ENSP00000448553.2:p.Phe903Leu
|
|
ENST00000549786.2:c.2165T>C
|
|
|
ENST00000647927.1:n.3110T>C
|
|
|
ENST00000648173.1:n.1532T>C
|
|
|
ENST00000648379.1:n.1105T>C
|
|
|
ENST00000648737.1:n.2501T>C
|
|
|
ENST00000648916.1:n.748T>C
|
|
|
ENST00000649607.1:c.921T>C
|
|
|
ENST00000650226.1:c.2737T>C
|
ENSP00000496981.1:p.Phe913Leu
|
|
ENST00000281928.7:c.2737T>C
|
ENSP00000281928.3:p.Phe913Leu
|
|
NM_015335.4:c.2737T>C
|
NP_056150.1:p.Phe913Leu
|
|
XM_011538080.1:c.2737T>C
|
XP_011536382.1:p.Phe913Leu
|
|
XM_011538081.1:c.2734T>C
|
XP_011536383.1:p.Phe912Leu
|
|
XM_011538082.1:c.2707T>C
|
XP_011536384.1:p.Phe903Leu
|
|
XM_011538080.2:c.2737T>C
|
XP_011536382.1:p.Phe913Leu
|
|
XM_011538081.2:c.2734T>C
|
XP_011536383.1:p.Phe912Leu
|
|
XM_011538082.2:c.2707T>C
|
XP_011536384.1:p.Phe903Leu
|
|
XM_017019090.1:c.2734T>C
|
XP_016874579.1:p.Phe912Leu
|
|
NM_015335.5:c.2737T>C
MANE Select
|
NP_056150.1:p.Phe913Leu
|
|