ENST00000312719.10:c.-339+41250T>G
(HS3ST5)
MANE Select
|
ENSP00000427888.1:n.-339+41250T>G
|
|
ENST00000312719.9:c.-339+41250T>G
(HS3ST5)
|
ENSP00000427888.1:n.-339+41250T>G
|
|
NR_125845.1:n.1800-39577A>C
(HDAC2-AS2)
|
|
|
XM_006715379.2:c.-339+41250T>G
(HS3ST5)
|
XP_006715442.1:n.-339+41250T>G
|
|
XM_011535587.1:c.-339+40427T>G
(HS3ST5)
|
XP_011533889.1:n.-339+40427T>G
|
|
XR_942347.1:n.239+41250T>G
(HS3ST5)
|
|
|
XM_017010470.1:c.-339+40427T>G
(HS3ST5)
|
XP_016865959.1:n.-339+40427T>G
|
|
XM_017010473.1:c.-335+40427T>G
(HS3ST5)
|
XP_016865962.1:n.-335+40427T>G
|
|
XM_017010474.2:c.-335+41250T>G
(HS3ST5)
|
XP_016865963.1:n.-335+41250T>G
|
|
NM_001387039.1:c.-227+40427T>G
(HS3ST5)
|
NP_001373968.1:n.-227+40427T>G
|
|
NM_001387040.1:c.-33+41250T>G
(HS3ST5)
|
NP_001373969.1:n.-33+41250T>G
|
|
NM_001387041.1:c.-335+41250T>G
(HS3ST5)
|
NP_001373970.1:n.-335+41250T>G
|
|
NM_001387042.1:c.-339+40427T>G
(HS3ST5)
|
NP_001373971.1:n.-339+40427T>G
|
|
NM_001387043.1:c.-335+40427T>G
(HS3ST5)
|
NP_001373972.1:n.-335+40427T>G
|
|
NM_001387044.1:c.-429+41250T>G
(HS3ST5)
|
NP_001373973.1:n.-429+41250T>G
|
|
NM_001387045.1:c.-434+41250T>G
(HS3ST5)
|
NP_001373974.1:n.-434+41250T>G
|
|
NM_001387046.1:c.-227+41250T>G
(HS3ST5)
|
NP_001373975.1:n.-227+41250T>G
|
|
NM_001387047.1:c.-434+40427T>G
(HS3ST5)
|
NP_001373976.1:n.-434+40427T>G
|
|
NM_153612.4:c.-339+41250T>G
(HS3ST5)
MANE Select
|
NP_705840.2:n.-339+41250T>G
|
|