|
ENST00000592784.6:c.1997A>T
(NLRP7)
MANE Select
|
ENSP00000468706.1:p.Asp666Val
|
|
|
ENST00000328092.9:c.1932-19A>T
(NLRP7)
|
ENSP00000329568.5:n.1932-19A>T
|
|
|
ENST00000340844.6:c.1997A>T
(NLRP7)
|
ENSP00000339491.2:p.Asp666Val
|
|
|
ENST00000586379.5:c.1997A>T
(NLRP7)
|
ENSP00000468243.1:p.Asp666Val
|
|
|
ENST00000588756.5:c.1997A>T
(NLRP7)
|
ENSP00000467123.1:p.Asp666Val
|
|
|
ENST00000590030.5:c.1997A>T
(NLRP7)
|
ENSP00000465520.1:p.Asp666Val
|
|
|
ENST00000592784.5:c.1997A>T
(NLRP7)
|
ENSP00000468706.1:p.Asp666Val
|
|
|
NM_001127255.1:c.1997A>T
(NLRP7)
|
NP_001120727.1:p.Asp666Val
|
|
|
NM_139176.3:c.1932-19A>T
(NLRP7)
|
NP_631915.2:n.1932-19A>T
|
|
|
NM_206828.3:c.1997A>T
(NLRP7)
|
NP_996611.2:p.Asp666Val
|
|
|
XM_006723075.2:c.1997A>T
(NLRP7)
|
XP_006723138.1:p.Asp666Val
|
|
|
XM_006723076.2:c.1997A>T
(NLRP7)
|
XP_006723139.1:p.Asp666Val
|
|
|
XM_011526596.1:c.2081A>T
(NLRP7)
|
XP_011524898.1:p.Asp694Val
|
|
|
XM_011526597.1:c.2081A>T
(NLRP7)
|
XP_011524899.1:p.Asp694Val
|
|
|
XM_011526598.1:c.2081A>T
(NLRP7)
|
XP_011524900.1:p.Asp694Val
|
|
|
XM_011526599.1:c.1997A>T
(NLRP7)
|
XP_011524901.1:p.Asp666Val
|
|
|
XM_011526600.1:c.1997A>T
(NLRP7)
|
XP_011524902.1:p.Asp666Val
|
|
|
XM_011526601.1:c.2081A>T
(NLRP7)
|
XP_011524903.1:p.Asp694Val
|
|
|
XM_011527530.1:c.*33T>A
(NCR1)
|
XP_011525832.1:n.*33T>A
|
|
|
XR_935761.1:n.2515A>T
(NLRP7)
|
|
|
|
XM_006723075.3:c.1997A>T
(NLRP7)
|
XP_006723138.1:p.Asp666Val
|
|
|
XM_006723076.3:c.1997A>T
(NLRP7)
|
XP_006723139.1:p.Asp666Val
|
|
|
XM_011526596.2:c.2081A>T
(NLRP7)
|
XP_011524898.1:p.Asp694Val
|
|
|
XM_011526599.2:c.1997A>T
(NLRP7)
|
XP_011524901.1:p.Asp666Val
|
|
|
XM_011526601.2:c.2081A>T
(NLRP7)
|
XP_011524903.1:p.Asp694Val
|
|
|
XM_011527530.3:c.*33T>A
(NCR1)
|
XP_011525832.1:n.*33T>A
|
|
