ENST00000593677.2:c.1683T>A
|
|
|
ENST00000688602.1:c.3080T>A
|
|
|
ENST00000689936.1:c.3052T>A
|
|
|
ENST00000692547.1:n.140T>A
|
|
|
ENST00000359596.8:c.14747T>A
MANE Select
|
ENSP00000352608.2:p.Val4916Asp
|
|
ENST00000355481.8:c.14732T>A
|
ENSP00000347667.3:p.Val4911Asp
|
|
ENST00000359596.7:c.14747T>A
|
ENSP00000352608.2:p.Val4916Asp
|
|
ENST00000360985.7:c.14729T>A
|
ENSP00000354254.4:p.Val4910Asp
|
|
NM_000540.2:c.14747T>A , LRG_766t1:c.14747T>A
|
NP_000531.2:p.Val4916Asp
|
|
NM_001042723.1:c.14732T>A
|
NP_001036188.1:p.Val4911Asp
|
|
XM_006723317.1:c.14729T>A
|
XP_006723380.1:p.Val4910Asp
|
|
XM_006723319.1:c.14714T>A
|
XP_006723382.1:p.Val4905Asp
|
|
XM_011527204.1:c.14744T>A
|
XP_011525506.1:p.Val4915Asp
|
|
XM_011527205.1:c.14660T>A
|
XP_011525507.1:p.Val4887Asp
|
|
XM_006723317.2:c.14729T>A
|
XP_006723380.1:p.Val4910Asp
|
|
XM_006723319.2:c.14714T>A
|
XP_006723382.1:p.Val4905Asp
|
|
XM_011527205.2:c.14660T>A
|
XP_011525507.1:p.Val4887Asp
|
|
NM_000540.3:c.14747T>A
MANE Select
|
NP_000531.2:p.Val4916Asp
|
|
NM_001042723.2:c.14732T>A
|
NP_001036188.1:p.Val4911Asp
|
|